Rocket Fuel Named One of Bay Area's Top Workplaces

REDWOOD SHORES, CA--(Marketwire -06/18/12)- Rocket Fuel, the leading provider of artificial intelligence advertising solutions for digital marketers, today announced it has been named one of the Bay Area's Top Workplaces.

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About Rocket Fuel:Rocket Fuel is the leading provider of artificial-intelligence advertising solutions that transform digital media campaigns into self-optimizing engines, which learn and adapt in real-time, and deliver outstanding results from awareness to sales. Recently awarded #22 in Forbes Most Promising Companies in America list, over 700 of the world's most successful marketers trust Rocket Fuel to power their advertising across display, video, mobile, and social media. Founded by online advertising veterans and rocket scientists from NASA, DoubleClick, IBM, and Salesforce.com, Rocket Fuel is based in Redwood Shores, California, and has offices in thirteen cities worldwide including New York, London, and Toronto.

2012 Rocket Fuel Inc. All rights reserved. Rocket Fuel Inc. is a registered trademark of Rocket Fuel Inc. in the U.S. and/or other countries. All other trademarks are the property of their respective owners.

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Rocket Fuel Named One of Bay Area's Top Workplaces

Where Advertising Meets Big Data: Rocket Fuel to Present at Stifel Nicolaus 2012 Internet & Media Conference

REDWOOD SHORES, CA--(Marketwire -06/18/12)- Rocket Fuel, the leading provider of artificial-intelligence advertising solutions for digital marketers, today announced that company co-founder and CEO George John will join a panel at the Stifel Nicolaus 2012 Internet & Media Conference at the New York Palace Hotel.

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About Rocket Fuel:Rocket Fuel is the leading provider of artificial-intelligence advertising solutions that transform digital media campaigns into self-optimizing engines, which learn and adapt in real-time, and deliver outstanding results from awareness to sales. Recently awarded #22 in Forbes Most Promising Companies in America list, over 700 of the world's most successful marketers trust Rocket Fuel to power their advertising across display, video, mobile, and social media. Founded by online advertising veterans and rocket scientists from NASA, DoubleClick, IBM, and Salesforce.com, Rocket Fuel is based in Redwood Shores, California, and has offices in thirteen cities worldwide including New York, London, and Toronto.

2012 Rocket Fuel Inc. All rights reserved. Rocket Fuel Inc. is a registered trademark of Rocket Fuel Inc. in the U.S. and/or other countries. All other trademarks are the property of their respective owners.

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Where Advertising Meets Big Data: Rocket Fuel to Present at Stifel Nicolaus 2012 Internet & Media Conference

Aeroports de Montreal, Bombardier Aerospace and Porter Airlines Kick-Off ICAO Flightpath to a Sustainable Future

MONTREAL, QUEBEC--(Marketwire -06/18/12)- Aeroports de Montreal (ADM), Bombardier Aerospace and Porter Airlines today joined forces to launch the inaugural flight of a series of biofuel flights which will deliver Raymond Benjamin, the Secretary General of the International Civil Aviation Organization (ICAO) to Rio de Janeiro for the United Nations Conference on Sustainable Development (Rio+20). Prior to departing from Montreal Pierre Elliott Trudeau International Airport to Billy Bishop Toronto City Airport, executives from each organization emphasized the importance of investing in sustainable aviation and their commitment to working with the industry to reduce the environmental impact of aviation.

"As signatories of the Aviation Industry Commitment to Action on Climate Change, we fully share these objectives," said Mr. James C. Cherry, President & CEO, Aeroports de Montreal. "I would like to take this opportunity to point out that Montreal-Trudeau airport was the first in North America to sell carbon credits and that we already have made several innovative achievements in the area of greenhouse gas reduction," added Mr. Cherry

This marks the second biofuel flight for Bombardier and Porter this year. In April, Porter successfully conducted the first biofuel-powered revenue flight in Canada. In the conclusion to a test program that was launched in 2010, the airline flew one of its Q400 turboprops from its base at Toronto City Airport to Ottawa using a 50/50 blend of biofuel and Jet A1 fuel in one of its engines. Today's flight is using the same fuel in one engine - certified to the new American Society for Testing and Materials (ASTM) D7566/D1655 standard and derived from the oilseed crop, Camelina sativa(i) (49 per cent) and Brassica carinata(i) (one per cent). The aircraft's other engine is powered by Jet A1 fuel.

The biofuel research is only one of many initiatives Bombardier has embarked on in recent years in the area of sustainable aviation as a pillar of the company's Corporate Social Responsibility program. Bombardier is also involved in numerous projects to reduce the environmental footprint of its sites and its products by using a lifecycle approach including Design for Environment and the implementation of Leadership in Energy and Environmental Design (LEED) building standards at its manufacturing sites.

"Bombardier is proud to be involved in this symbolic journey for the industry," said Helene V. Gagnon, Vice-President, Public Affairs, Communications and Corporate Social Responsibility, Bombardier Aerospace. "As a leading aircraft manufacturer we must act as a role model for the industry where the environment is concerned, not only by designing and building innovative and responsible products, but by working in partnership with the entire industry to find solutions that can benefit us all in the long term."

Porter operates a single-type fleet of 26 Q400 aircraft throughout its regional network.

"One reason that Porter initially chose the Q400 aircraft is because of its efficiency characteristics, including substantially reduced fuel usage and emissions compared to comparable jet aircraft," said Robert Cordes, Executive Vice President and COO, Porter Airlines. "Biofuel used on a regular basis has the potential to make even greater improvements in the future. We're proud to contribute to this goal as part of overall industry efforts."

About Q400 aircraf

The Q400 turboprop airliner, which is built at Bombardier's Toronto, Ontario facility, is the advanced successor to Bombardier's Dash 8/Q-Series family of aircraft. Optimized for short-haul operations, the "comfortably greener," 70- to 80-seat Q400 aircraft is a large, fast, quiet and fuel-efficient turboprop. It provides an ideal balance of passenger comfort and operating economics with a reduced environmental footprint.

Setting new environmental standards, the Q400 aircraft uses 30 to 40 per cent less fuel and produces 30 to 40 per cent fewer emissions on routes where it has replaced similar-capacity, older jets. Overall, the Q400 aircraft is 15 decibels quieter than ICAO Chapter 4 noise standards; raising the bar for the entire industry.

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Aeroports de Montreal, Bombardier Aerospace and Porter Airlines Kick-Off ICAO Flightpath to a Sustainable Future

Bombardier buys land in Casablanca free zone for aerospace manufacturing plant

By Ross Marowits, The Canadian Press

MONTREAL - Bombardier Aerospace says it has bought land near the airport in Casablanca's free zone that offers five years of no taxes and other financial incentives for a manufacturing facility set to open next year.

The Montreal-based aircraft manufacturer said Monday it signed a deal with Moroccan property holding and management company Midparc Investment S.A. for the land in a free zone in Nouaceur.

Midparc is owned by a state financial agency and three private industrial companies specializing in aeronautics and electronics fields.

Bombardier Aerospace president Guy Hachey said the selection of the site for the manufacturing facility is "an important first step" in establishing the world's third-largest aircraft manufacturer in the North African country.

"The site met our stringent requirements and high standards and we look forward to the start of the construction and production of the first Moroccan-built Bombardier aircraft components," he stated in a news release.

Hachey said it hopes the long-term relationship will serve as a catalyst for the aircraft industry in Morocco.

Bombardier (TSX:BBD-B.TO - News) joins other aerospace manufacturers in setting up shop in Morocco, which has established an aerospace training program and offers many tax and financial incentives to attract companies.

The company will pay no taxes for five years, 8.75 per cent for another 20 years and 17.5 per cent thereafter.

On its website, Midparc boasts about low wages being one of Morocco's advantages. It said the average monthly wage is US$327, lower than in Tunisia and Turkey, 10 times lower than Spain and a quarter of what's earned in South Africa.

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Bombardier buys land in Casablanca free zone for aerospace manufacturing plant

CepMed Appoints New CEO

MONTREAL, QUEBEC--(Marketwire -06/18/12)- Mr. Michel Saucier, Chairman of the Board of Directors of CepMed, the Center of Excellence in Personalized Medicine, is pleased to announce the appointment of Ms. Manon Decelles, CPA, CGA as Chief Executive Officer. Coincident with Ms. Decelles' arrival, Dr. Clarissa Desjardins, outgoing CEO, is leaving to manage a start-up biotechnology company.

Ms. Decelles has 20 years of experience in the pharmaceutical industry and a proven track record in key areas of business including finance, marketing and business development. Together with this experience Ms. Decelles brings an extensive business network that will enable CepMed in bringing together medical, scientific and business communities to promote innovation and commercialization in personalized medicine. Prior to joining CepMed, Ms. Decelles was Director of Business Development and Acquisitions at Sanofi, a global and diversified healthcare leader, where she was responsible for the Canadian affiliate's business development activities, including in and out licensing, divestitures as well as company acquisitions. In this capacity, Ms. Decelles developed and implemented a Strategic Business Development Plan and review process that guided Sanofi's Canadian strategy. Previously, Ms. Decelles held roles of increasing responsibility in finance, marketing and business development at Marion Merrell Dow, Hoechst Marion Roussel and Aventis. Ms. Decelles is an active member of the Board of Directors of the Canadian Healthcare Licensing Association.

Ms. Decelles first studied in science - microbiology at the University of Sherbrooke. She later obtained a Bachelor of Business Administration from the University of Montreal, HEC and is also a Chartered Professional Accountant (CPA).

"As Cepmed approaches its fifth year of operations, we believe that Manon's background and experience is perfectly suited to take Cepmed to the next level. Going forward, we expect to increasingly attract foreign investment in our centre for translational studies, commercialize the results of our studies and implement personalized medicine tests and strategies into our healthcare system. We welcome Manon to her new position and are confident that she can take on this challenge." - Mr. Michael Saucier, Chairman of the Board, CepMed

The Board extends its best wishes to Clarissa in her new endeavors and its deep gratitude for her contributions to CepMed and the advancement of personalized medicine in Canada. "Her leadership of our public-private partnerships and innovative knowledge translation activities including a Personalized Medicine Portal and the creation of physician's expert panels in cardiology, oncology and family medicine have created an awareness of personalized medicine and its benefits across the country." - Dr. Jean Claude Tardif, Director Montreal Heart Institute Research Centre

About CepMed

Founded by the Montreal Heart Institute and Genome Quebec in 2008, CepMed is a non-profit organization dedicated to promoting the science and practice of personalized medicine. It is a Centre of Excellence for Commercialization and Research (CECR) funded by the Canadian Government, Genome Quebec and industry partners including Pfizer, AstraZeneca, Novartis and Merck. Cepmed's initiatives are designed to promote and enable personalized medical treatment, based on the use of molecular information in clinical decision making, in particular to improve the efficacy and safety of drug therapy. Cepmed participates in several multi-million dollar public-private partnerships (PPP) in translational medicine that incorporate pharmacogenomics into Phase III clinical trials or studies of marketed drugs with partners including Roche and Servier. These partnerships leverage the expertise and capacities of The Beaulieu Saucier Pharmacogenics (PGx) Centre, The Montreal Heart Institute Coordinating Centre (MHICC) and The Montreal Heart Institute Biobank. Generating several millions of dollars in investment these partnerships have established a unique and world class centre for translational clinical research. In addition CepMed is collaborating and partnering with Canadian stakeholders in personalized medicine including physicians, patients, governments, industry and investors to enable the clinical development and implementation of personalized medicine while creating commercial opportunities for Canadian companies.

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CepMed Appoints New CEO

Research and Markets: Argentina Neurology Devices Market Outlook to 2018 – Interventional Neurology, Neurological …

DUBLIN--(BUSINESS WIRE)--

Research and Markets (http://www.researchandmarkets.com/research/nlp2hj/argentina_neurolog) has announced the addition of GlobalData's new report "Argentina Neurology Devices Market Outlook to 2018 - Interventional Neurology, Neurological Diagnostic Equipment, Neurostimulation Devices and Others" to their offering.

GlobalData's new report provides key market data on the Argentina Neurology Devices market. The report provides value (USD million), volume (units) and average price (USD) data for each segment and sub-segment within six market categories - CSF Management, Interventional Neurology, Neurological Diagnostic Equipment, Neurostimulation Devices, Neurosurgical Products and Radiosurgery. The report also provides company shares and distribution shares data for each of the aforementioned market categories. The report is supplemented with global corporate-level profiles of the key market participants with information on company financials and pipeline products, wherever available.

This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData's team of industry experts.

Scope:

- Market size and company share data for Neurology Devices market categories - CSF Management, Interventional Neurology, Neurological Diagnostic Equipment, Neurostimulation Devices, Neurosurgical Products and Radiosurgery.

- Annualized market revenues (USD million), volume (units) and average price (USD) data for each of the segments and sub-segments within six market categories. Data from 2004 to 2011, forecast forward for 7 years to 2018.

- 2011 company shares and distribution shares data for each of the six market categories.

- Global corporate-level profiles of key companies operating within the Argentina Neurology Devices market.

- Key players covered include Medtronic, Inc., Nihon Kohden Corporation, St. Jude Medical, Inc., Stryker Corporation, Cadwell Laboratories, Inc., DePuy, Inc. and others.

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Research and Markets: Argentina Neurology Devices Market Outlook to 2018 - Interventional Neurology, Neurological ...

Research and Markets: France Neurology Devices Market Outlook to 2018 – Interventional Neurology, Neurological …

DUBLIN--(BUSINESS WIRE)--

Research and Markets (http://www.researchandmarkets.com/research/q5ctlz/france_neurology_d) has announced the addition of GlobalData's new report "France Neurology Devices Market Outlook to 2018 - Interventional Neurology, Neurological Diagnostic Equipment, Neurostimulation Devices and Others" to their offering.

This new report provides key market data on the France Neurology Devices market. The report provides value (USD million), volume (units) and average price (USD) data for each segment and sub-segment within six market categories - CSF Management, Interventional Neurology, Neurological Diagnostic Equipment, Neurostimulation Devices, Neurosurgical Products and Radiosurgery. The report also provides company shares and distribution shares data for each of the aforementioned market categories. The report is supplemented with global corporate-level profiles of the key market participants with information on company financials and pipeline products, wherever available.

This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData's team of industry experts.

Scope:

- Market size and company share data for Neurology Devices market categories - CSF Management, Interventional Neurology, Neurological Diagnostic Equipment, Neurostimulation Devices, Neurosurgical Products and Radiosurgery.

- Annualized market revenues (USD million), volume (units) and average price (USD) data for each of the segments and sub-segments within six market categories. Data from 2004 to 2011, forecast forward for 7 years to 2018.

- 2011 company shares and distribution shares data for each of the six market categories.

- Global corporate-level profiles of key companies operating within the France Neurology Devices market.

- Key players covered include Medtronic, Inc., St. Jude Medical, Inc., Accuray Incorporated, Stryker Corporation, Cadwell Laboratories, Inc., B. Braun Melsungen AG and others.

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Research and Markets: France Neurology Devices Market Outlook to 2018 - Interventional Neurology, Neurological ...

Medical Marijuana Inc. Advisory Committee and Board of Directors Update

SAN DIEGO, June 18, 2012 /PRNewswire/ --Medical Marijuana Inc. (MJNA) a leading cannabis and hemp industry innovator, is pleased to announce the appointment of the CanCHEW Bio-technologies executive team Dr. George Anastassov, Dr. Philip A. Van Damme and Lekhram Changoer to its Board of Directors and Medical Advisory Committee.

Dr. George E. Anastassov, Director

George E. Anastassov, MD, DDS, graduated with BA Degree, Fine Arts School, Sofia, Bulgaria in 1981, followed by MD Degree, Medical Academy, Higher Medical Institute Sofia, Bulgaria, and a DDS Degree, New York University College of Dentistry, New York, New York In 1990.

Between 1988 and 1991 held Clinical Extern positions at the, Department of Oral and Maxillofacial Surgery, Bellevue Hospital Centre, New York. Clinical Assistant, Department of Plastic and Reconstructive Surgery and Microsurgery, Memorial Sloan-Kettering Cancer Centre, New York, and Clinical Extern, at the Department of Oral and Maxillofacial Surgery, Bellevue Hospital Centre, New York.

Operating in private practice between 1990 1993 and with a longer term private practice role between 1991 1999 at East Village Dental Group. New York, N.Y. Dr Anastassov additionally executed various post doctoral education positions notably; A Fellowship in Cranio-Maxillofacial Surgery. (Professor H.P.M. Freihofer), The Catholic University, St. Radboud Hospital, Nijmegen, the Netherlands 1994. Chief Resident, Department of Oral and Maxillofacial Surgery, Montefiore Medical Centre, Albert Einstein College of Medicine, Bronx, New York between June 1995 and June 1996. Followed by a further Fellowship in Craniofacial and Base of Skull Surgery, at the department of Cranio-Maxillofacial and Plastic and Reconstructive Surgery, Wilhelms University, Munster, Germany between June 1996 and June 1997.

Eventually returning to a variety of Hospital appointments in the US between 1997 - 2007: including Associate Director, Department of Maxillofacial Surgery, Elmhurst Hospital Centre, Queens, N.Y. Assistant-Attending, Department of Dentistry, The Mount Sinai Hospital. New York. Consultant in Maxillofacial Surgery, Bronx VA Hospital Centre, Bronx, N.Y. 1997 - present, and three additional ongoing roles, Attending, Department of Maxillofacial Surgery, Elmhurst Hospital Centre, Queens, N.Y. Attending, Department of Dentistry, the Mount Sinai Hospital. New York, N.Y. Attending Surgeon, Department of Otolaryngology/ Head and Neck Surgery, Beth Israel Medical Centre, New York. Visiting Professor, Department of Crania-Maxillofacial Surgery and Plastic and Reconstructive Surgery, Wilhelm's University, Munster, Germany. Associate Clinical Professor of Oral and Maxillofacial Surgery. The Mount Sinai School of Medicine.

Editorially, Dr. Anastassov is presently active as Editorial Consultant 'The Journal of Oral Surgery, Oral Medicine, Oral Pathology and Radiology'. Editorial Board Member 'International Journal of Oral and Maxillofacial Surgery' Since 2000. And also Editorial Board Member 'Folia Medica' and Editorial Consultant - 'Head and Face Medicine'.

Dr. Anastassov was granted Fellowship to the American College of Oral and Maxillofacial Surgeons in 2000 and Fellowship to the American College of Dentistry in 2005, and with Chairman appointments during the First International Congress of the Cleft Lip and Palate Foundation "Cleft 2000", Chairman, Facial Aesthetics Section. XV Congress of the European Association for Cranio-Maxillofacial Surgery. Edinburgh, UK, September 5-9, 2000 and Chairman, Aesthetic Surgery. XVI Confidential Executive Summary_Sanammad_25102010 14 Congress of the European Association for Cranio-Maxillofacial Surgery. Munster, Germany, September 3-7, 2002.

Dr. Anastassov holds 9 US & European Professional Society Membership: including a certified member of American Board of Oral and Maxillofacial Surgery, additionally with 43 journal publications and 75 international guest lecture's to his credit.

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Medical Marijuana Inc. Advisory Committee and Board of Directors Update

Braun: Rutgers-Camden medical school situation is personal, as well as political

Add yet another factor to the emotional politics behind the drive to strip Rutgers University of control over its Camden campus, politics described by one state senator as "the beginning of a new civil war": The personal. The rejection that the powerful Norcross family of South Jersey felt at the refusal of the universitys president to take over the new Cooper Medical School in Camden.

"Rutgers could have had the medical school some years ago," said State Sen. Donald Norcross (D-Camden), the prime sponsor of the bill that aims to "reorganize" higher education in the state but also results in the first real threat to the autonomy and structural integrity of Rutgers University in its 56-year history as it is called under the law, "The State University of New Jersey."

"For whatever reason, they decided not to," said Norcross, whose brother George is political boss of South Jersey.

Through the efforts of Senate President Steve Sweeney (D-Gloucester) and the demands of Gov. Chris Christie, the bill is racing through the Legislature without so much as a pause to think of its price tag. The other day, the five senators on the Senate Higher Education committee voted for the bill, although the three Democrats and two Republicans admitted like Donald Norcross did they had no clue how much money it would cost. Critics have put the price at a quarter-billion dollars, maybe more.

Donald Norcross blamed the Rutgers "bureaucracy" for rejecting Cooper Medical School, but that bureaucracy is headed at least until the end of the month by outgoing president Richard McCormick.

McCormick, despite the reluctance of his governing boards and the opposition of faculty and many students, has pushed hard for the part of the bill that permits the universitys takeover of the Central Jersey operations of the University of Medicine and Dentistry of New Jersey (UMDNJ) even at the price of losing the Camden campus. Rutgers briefly had a medical school until 1971 when the state took it over as part of UMDNJ; regaining it would be McCormicks legacy.

The bill, as written by Sweeney, adds another sweetener the Rutgers takeover of UMDNJs Newark assets, giving Rutgers two medical school campuses. That part of the bill led to the comment about "civil war" when state Sen. Ronald Rice (D-Essex) implored the committee to hold the bill.

But the unanswered question hanging over the legislative hearings and the entire proposal is this: If it is good state policy for New Jerseys state university to take over medical education in Newark and Piscataway, why not in Camden?

Donald Norcross, in an interview after he testified before the Senate Higher Education Committee, answered: "Why would we want to empower Rutgers to take over an asset of Rowan University?"

Rowan University, a former state teachers college whose biggest major is still teacher education, had agreed to take in the medical school after McCormick declined. "Rowan has done a good job," Norcross said.

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Braun: Rutgers-Camden medical school situation is personal, as well as political

Scientists Create First Genetically Evolved Chip Material

There may be an unexpected solution for the challenge of shrinking transistor sizes.

Researchers at the University of California, Santa Barbara, say they have succeeded in growing new mineral architectures by "directing the evolution" silicateins, which are the proteins responsible for the formation of silicon skeletons in marine sponges. For the first time, it was shown that it is possible to develop the enzymatic synthesis of a semiconductor using genetic engineering and molecular evolution. The implication? Companies may be able to use DNA information to develop their own "specialized" materials.

The key to the research was the use of silicateins, which are genetically encoded and are used as a blueprint for the creation of silica skeletons. According to the UCSB researchers, the process is very similar to the way animal and human bones are formed. In their study, polystyrene microbeads coated with specific silicateins were "put through a mineralization reaction by incubating the beads in a water-in-oil emulsion that contained chemical precursors for mineralization." As the silicateins reacted with the dissolved metals, "they precipitated them, integrating the metals into the resulting structure and forming nanoparticles of silicon dioxide or titanium dioxide." The result was the creation of a silicatein gene pool that enabled the researchers to pick silicateins with the specific properties they were looking for.

"This genetic population was exposed to two environmental pressures that shaped the selected minerals: The silicateins needed to make materials directly on the surface of the beads, and then the mineral structures needed to be amenable to physical disruption to expose the encoding genes," said Lukmaan Bawazer, the author a corresponding paper that is published in the current issue of the journal Proceedings of the National Academy of Sciences.

"The beads that exhibited mineralization were sorted from the ones that didn't, and then fractured to release the genetic information they contained, which could either be studied, or evolved further."

Bawazer said that he is now trying to evolve to evolve the research result into a functional device.

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Scientists Create First Genetically Evolved Chip Material

Real-time gene sequencing used to fight MRSA

LONDON Scientists have used genome sequencing technology to control an outbreak of the superbug MRSA in a study that could point to faster and more efficient treatment of a range of diseases.

The work adds to a burgeoning body of research into better techniques for diagnosing disease more quickly and at an earlier stage to allow more effective treatment and reduce health care costs.

Much of this is being driven by whole genome sequencing, which has enabled scientists to identify the genetic markers for a range of afflictions.

MRSA, or Methicillin-Resistant Staphylococcus Aureus, is a drug-resistant bacterial infection, or superbug, and major public health problem. When outbreaks occur in hospitals it can lead to the closure of whole wards and lengthy investigations.

The bug kills an estimated 19,000 people in the United States alone each year, and even when the infection is successfully treated it can double the average length of a hospital stay and thereby increase health care costs.

A team of scientists from the Wellcome Trust Sanger Institute, the University of Cambridge and genome sequencing company Illumina Inc, used samples from a 2009 MRSA outbreak in a hospital neo-natal intensive care ward to recreate and respond to it, as if in real time.

They found that genome sequencing produced results in roughly 24 hours, using the latest technology from Illumina, gave much more detailed information.

The researchers were able to identify the particular strain of MRSA causing the outbreak, and which strains were not, quickly enough to feed back into treatment and nip the outbreak in the bud faster than current clinical testing methods.

"I think we are at the very beginning of an explosion of evidence to support the use of whole genome sequencing in public health," Sharon Peacock of Cambridge University, who led the study, told Reuters.

The research, published in the New England Journal of Medicine, comes hot on the heels of similar work done on MRSA and Clostridium difficile by a team from Oxford University with Illumina and a group of hospitals in Britain.

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Real-time gene sequencing used to fight MRSA

EPA Honors 2012 Presidential Green Chemistry Challenge Award Winners

*EPA Honors 2012 Presidential Green Chemistry Challenge Award Winners*

WASHINGTON June 18, 2012: Today the U.S. Environmental Protection Agency recognized innovative chemical technologies that have the potential to prevent pollution in the United States. These awards recognize leading researchers and industrial innovators who create safer and more sustainable chemical designs, processes, and products that reduce the need to use chemicals that pollute the environment and threaten Americans' health. The awardees were honored during the 17th Annual Green Chemistry Challenge Awards Ceremony in Washington, D.C.

"EPA congratulates the 2012 winners for designing, developing, and implementing these innovative green chemistry technologies that will help create more sustainable industries and greener, safer products to protect people's health and the environment," said Jim Jones, EPA's acting assistant administrator for the Office of Chemical Safety and Pollution Prevention. "These are exciting technologies that have great potential to improve the safety of the detergents and personal care products we use in our homes; reduce energy consumption and hazardous waste in industrial metal production processes; improve the paper goods and plastics we use daily so that they are made with a smaller environmental footprint and can be recycled more effectively; and even a potential alternative to BPA-based can linings,"

The Presidential Green Chemistry Challenge Awards include five categories: Academic, Small Business, Greener Synthetic Pathways, Greener Reaction Conditions and Designing Greener Chemicals.

This year, EPA is recognizing two winning academic technologies: Robert M. Weymouth, PhD, Stanford University, Stanford, Calif., and James L. Hedrick, PhD, San Jose, Calif., for organic catalysis -- an innovation that removes hazardous metals used in the production of plastics. The technique creates a safer end product that allows bottle-to-bottle recycling, thereby providing an opportunity to reduce the millions of pounds of plastics that end up in landfills.

Geoffrey W. Coates, PhD, Cornell University, Ithaca, N.Y., for synthesizing biodegradable polymers from carbon dioxide and carbon monoxide that can be used in a wide range of adhesives, foams, plastic and potentially lead to the development of a BPA-alternative for use in can linings.

In the small-business category, Elevance Renewable Sciences, Inc., Woodridge, Ill., is being recognized for the production of high-performing, green specialty chemicals at advantageous costs. These green chemicals can be produced with less energy, significantly reduced greenhouse gas emissions compared to petrochemical technologies, and used in a wide range of consumer and industrial products and processes.

Winners in the "Greener Reaction Conditions, Designing Greener Chemicals, and Greener Synthetic Pathways," categories include:

Cytec Industries Inc., Woodland Park, N.J. for MAX HT "Bayer Process" scale inhibitor products that result in a drastically more energy efficient and less hazardous process for the production of alumina, a raw material for making aluminum. Application of this technology can result in reducing hazardous acid waste by millions of pounds annually and preventing billions of pounds of CO2 from being released into the atmosphere.

Buckman International, Inc., Memphis, Tenn., for enzymes to be used in papermaking that modify the cellulose in wood to increase the number of "fibrils" that bind the wood fibers to each other. The innovation produces paper with improved strength and quality without additional chemicals or energy. The process also allows papermaking with less wood fiber and higher percentages of recycled paper, enabling a single plant to save $1 million per year.

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EPA Honors 2012 Presidential Green Chemistry Challenge Award Winners

Covance Appoints Dr. Steve Street to Lead Worldwide Safety Assessment and Pharmaceutical Chemistry Services

PRINCETON, N.J., June 18, 2012 /PRNewswire/ -- Covance Inc. (CVD) today announced that Steve Street, Ph.D., has joined the company as Global Vice President and General Manager, overseeing Covance's worldwide safety assessment and pharmaceutical chemistry services. He will be based in Harrogate, UK.

Dr. Street, with more than 27 years of experience in biopharmaceutical R&D, joins Covance from Pfizer, Inc., where he served as Vice President and Head of two global R&D units the Research Centers of Emphasis and Continuous Improvement. In these roles, he led the company's high-performing technology and operations group to increased portfolio development speed and project survival, ultimately creating a positive impact across multiple therapeutic areas, including chemistry and biology outsourcing, innovation, and new indications. During his tenure at Pfizer, Dr. Street also served as Head of the company's Worldwide Chemistry Discipline.

"Steve's keen strategic insights and exceptional R&D background will benefit Covance as we refine our global presence and strengthen our scientific expertise in early development," said Deborah Tanner, Executive Vice President and Group President, R&D Laboratories, Covance. "Science is at the core of everything we do, and the addition of a leader like Steve allows us to continue to meet clients' needs in this increasingly complex industry and, ultimately, remain the drug development partner of choice."

"Covance is known for its continuous global innovation in development, superior quality of products and services, and long-standing client relationships, all of which are essential elements for sustained success in today's highly competitive R&D landscape," said Dr. Street. "With an increasing focus on outsourcing, this is a very exciting time to transition from pharma to a contract research organization, and I am proud to join the industry leader. I look forward to learning from and working with a talented, dedicated group of new colleagues at Covance."

Dr. Street is a Fellow of the Royal Society of Chemistry, a member of the American Chemical Society, and recently served as a visiting Professor of Chemistry at the University of Nottingham, UK. He received a doctorate from Leeds University in the UK.

Covance generates more new drug development data than any other organization in the world. The company offers the industry's broadest and most integrated portfolio of R&D services, offering flexible, milestone-based solutions and full development solutions in clinical pharmacology, early clinical development, and molecule development.

About Covance

Covance, with headquarters in Princeton, New Jersey, is one of the world's largest and most comprehensive drug development services companies, with annual revenues greater than $2 billion, global operations in more than 30 countries, and more than 11,000 employees worldwide. Information on Covance's products and services, recent press releases, and SEC filings can be obtained through its website at http://www.covance.com.

Forward Looking Statements

Statements contained in this press release (and in the webcast announced in this press release), which are not historical facts, such as statements about prospective earnings, savings, revenue, operations, revenue, earnings growth, and other financial results are forward-looking statements pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All such forward-looking statements including the statements contained herein regarding anticipated trends in the Company's business are based largely on management's expectations and are subject to and qualified by risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include factors described in the Company's filings with the Securities and Exchange Commission including its Annual Report on Form 10-K and Quarterly Reports on Form 10-Q. The Company undertakes no duty to update any forward looking statement to conform the statement to actual results or changes in the Company's expectations.

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Covance Appoints Dr. Steve Street to Lead Worldwide Safety Assessment and Pharmaceutical Chemistry Services

Emma Stone had instant chemistry with Andrew Garfield

People News

Jun 18, 2012, 22:01 GMT

Andrew Garfield and Emma Stone

Emma Stone and Andrew Garfield had 'instant chemistry'.

The couple began dating after meeting on the set of 'The Amazing Spider-Man' and the actress loved working closely with the actor on the superhero movie and hoped their close bond is reflected in their characters.

Emma - who plays Gwen Stacy - said: 'It was really great to work with Andrew. We just had instant chemistry as soon as we were on set and I think it was great to be able to build that relationship.'

Emma has previously worked with hunky actors including Penn Badgley in 'Easy A' and Ryan Gosling in 'Crazy, Stupid, Love' and jokingly claimed she only agrees to appear in films with 'hot' co-stars.

Speaking at the UK premiere of 'The Amazing Spider-Man' in London's Leicester Square this evening (18.06.12), she told BANG Showbiz: 'I only seem to work with hot men and it''s pretty great to get that contractually written.'

The 23-year-old beauty also admitted she much prefers the 'romance' element to 'The Amazing Spider-Man' as she was more comfortable shooting those scenes than getting to grips with anything physical.

She said: 'The romance is my favourite part of filming because I don't do the action quite as well.'

Original post:
Emma Stone had instant chemistry with Andrew Garfield

Advancing Global Green Chemistry — The role of government, business and academia

Public release date: 18-Jun-2012 [ | E-mail | Share ]

Contact: Joan Coyle J_coyle@acs.org 202-872-6229 American Chemical Society

WASHINGTON, June 18, 2012 News media and others interested in advancing the role of green chemistry can join a panel discussion on Wednesday, June 20, during the 16th annual Green Chemistry & Engineering Conference. From 9:30 to 11:45 a.m. (EDT) the American Chemical Society Green Chemistry Institute (ACS GCI) will provide live streaming video of "Advancing Global Green Chemistry The Role of Government, Business and Academia." To participate, click here.

This free event will allow ACS GCI to utilize state-of-the-art technology to further enhance the profile and importance of green chemistry while linking the global green chemistry community. All green chemistry enthusiasts, including chemists, engineers, researchers, policy analysts, managers/directors, venture capitalists, chemistry and engineering students, chemistry and business school professors and others are encouraged to participate.

Panelists Include:

Each panelist will provide a 15-minute presentation followed by a 10-minute question-and-answer session. Virtual audience members will submit questions for the panelists via a secure web server, and a moderator will assist the panelists with the flow of questions and responses.

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Please click here to register. Advance registration enables attendees to submit questions before the session and to receive a reminder email and password the day before the session.

The American Chemical Society is a nonprofit organization chartered by the U.S. Congress. With more than 164,000 members, ACS is the world's largest scientific society and a global leader in providing access to chemistry-related research through its multiple databases, peer-reviewed journals and scientific conferences. Its main offices are in Washington, D.C., and Columbus, Ohio.

The ACS Green Chemistry Institute is an organization focused on catalyzing and enabling the implementation of green chemistry and engineering throughout the global chemical enterprise. ACS GCI operates industrial roundtables; conducts conferences, seminars and training; maintains an international network of 26 green chemistry chapters; and with its partner NSF International, led the effort to establish the first consensus standard for greener chemical products and process information in the United States.

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Advancing Global Green Chemistry -- The role of government, business and academia

Encycle Therapeutics Launches Ground-Breaking Chemistry Platform

Platform for cyclizing peptides promises to increase efficiency of early-stage drug discovery

BOSTON , June 18, 2012 /CNW/ - Encycle Therapeutics, a MaRS Innovation spin-off company, has created a ground-breaking chemistry platform for cyclizing peptides that promises to increase the efficiency of the early-stage drug discovery process.

Peptides have long been sought after as therapeutics due to their high specificity they can hit specific cellular targets, especially complex protein-protein interaction targets implicated in cancer, cardiovascular disease and metabolic disorders.

In their linear form, however, peptides are unstable. When used as drug-delivery agents, they break down before reaching therapeutic targets or fail to permeate cell walls, presenting a long-standing challenge to medicinal chemists.

Encycle's breakthrough chemistry platform stabilizes linear peptides for drug development by cyclizing them. This process has demonstrably increased the drug-like properties of these molecules, increasing their stability in the body and providing a higher degree of cell permeability. The platform adapts to any linear peptide input and has the power to generate libraries of compounds to facilitate drug discovery and development.

This technology, discovered in Professor Andrei Yudin 's chemistry laboratory at the University of Toronto , will be developed with the collaboration of Professor Eric Marsault, specialized in medicinal chemistry at the Institut de Pharmacologie de Sherbrooke of Universit de Sherbrooke. Together, they will demonstrate that Encycle's foundational chemistry technology functions for a wide variety of peptides and that the platform can hit therapeutic targets of interest. Encycle will then be well positioned to pursue discovery-stage relationships with the pharmaceutical partners involved in the project around targets of their choosing.

"It costs over $1 billion to bring a new drug to market under the current high through-put pharmaceutical discovery model," says Yudin, professor of Chemistry at U of T and Encycle Founder. "Instead of randomly searching millions of compounds, Encycle's platform will allow us to design a peptide molecule with small molecule properties, such as stability and cell permeability, while remaining more likely to interact with a targeted therapeutic area. In theory, this approach would save time, money and reduce overhead risk."

"The approach pioneered by Andrei Yudin is remarkable for its efficiency in the synthesis of macrocycles, which are otherwise very difficult to reach and thus difficult to exploit in drug discovery," says Marsault. "This collaboration will unlock the potential of this class and provide much-needed new classes of drug candidates able to mimic the natural structural elements of proteins."

"This innovative project is a successful result of our established commitment towards technology transfer of excellent research and partnering with the private and public sectors," says Jacques Beauvais , vice-rector of research at the Universit de Sherbrooke.

The project has received $1 million in seed funding, largely derived through The Qubec Consortium for Drug Discovery's funding programs, and has attracted interest from four pharmaceutical companies.

Read more here:
Encycle Therapeutics Launches Ground-Breaking Chemistry Platform

Cytec Wins EPA Presidential Green Chemistry Award

Cytec Wins EPA Presidential Green Chemistry Award

Woodland Park, New Jersey, June 18, 2012 - Today, Cytec Industries Inc. (CYT) was awarded the top honor in green chemistry, the Presidential Green Chemistry Challenge Award. The award, created by the Environmental Protection Agency (EPA), recognizes companies that have pioneered sustainable technologies that incorporate the principles of green chemistry. Cytec`s MAX HT scale control technology enables greener conditions within the Bayer process, a process used for converting bauxite ore to alumina, the primary raw material for aluminum. The innovation reduces pollution at the source in addition to reducing energy use and waste generation. "Cytec has been a pioneer in developing innovative solutions for the mining industry while maintaining a focus on sustainable technologies. We are honored to receive such a prestigious award from the EPA," said Shane Fleming, Cytec`s Chairman, President, and CEO.

Today`s green chemistry award recognizes one of the many technology innovations Cytec has achieved within its In Process Separation business segment. MAX HT Bayer Sodalite Scale Inhibitor is the first scale inhibitor product in the market for this application and solves a legacy production challenge within the alumina industry. This technology provides benefits by reducing or eliminating the scale formation in heat exchangers resulting in higher heat transfer rates while reducing energy consumption and waste generation. "The realized energy saving for the combined customers currently utilizing our MAX HT technology is approximately 47 trillion Btu, which is the equivalent of up to 8 billion pounds of carbon dioxide (CO2) not released to the atmosphere," said Martin Court, Cytec`s Vice President, In Process Separation business. Martin added, "Fewer cleaning cycles also result in a realized annual hazardous waste reduction of up to 200 million pounds in total for all of the current operations using this product."

Cytec`s sustainability strategy is focused on developing innovative and environmentally sustainable products that compete in a global economy; achieving the highest standards of safety, health and environmental stewardship and operational excellence. The company uses business-specific market drivers and best practices to drive the sustainability efforts.

Corporate Profile Cytec`s vision is to deliver specialty chemical and material technologies beyond our customers` imagination. Our focus on innovation, advanced technology and application expertise enables us to develop, manufacture and sell products that change the way our customers do business. Our pioneering products perform specific and important functions for our customers, enabling them to offer innovative solutions to the industries that they serve. Our products serve a diverse range of end markets including aerospace composites, structural adhesives, automotive and industrial coatings, electronics, inks, mining and plastics.

Contact: Jodi Allen Communications and Investor Relations (973) 357-3283

The owner of this announcement warrants that: (i) the releases contained herein are protected by copyright and other applicable laws; and (ii) they are solely responsible for the content, accuracy and originality of the information contained therein.

Source: Cytec Industries Inc via Thomson Reuters ONE HUG#1620380

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Cytec Wins EPA Presidential Green Chemistry Award

BIO Applauds Rep. Kaptur’s Energy Investment Act of 2012

WASHINGTON--(BUSINESS WIRE)--

The Biotechnology Industry Organization (BIO) today thanked Rep. Marcy Kaptur (D-Ohio) and 16 other original cosponsors for introducing the Rural Energy Investment Act of 2012, which would reauthorize Farm Bill Energy Title programs, provide significant mandatory funding, and ensure eligibility for additional biorefineries and products, such as biobased products and renewable chemicals. BIO President & CEO Jim Greenwood released the following statement:

I agree with Representative Kaptur that Farm Bill energy programs are working. The programs have had a tremendous positive impact in revitalizing rural America, helping new agricultural markets emerge, and reducing the need for direct payments to farmers. Through these programs, companies are unlocking private capital for construction of the nations first cellulosic and advanced biofuel biorefineries; and farmers in 12 states are putting more than 160,000 acres of underutilized farmland back into production raising next generation energy crops. There has also been an explosion of renewable chemicals innovation, demonstration and early commercialization here in the United States, and Representative Kapturs bill would support its continued momentum.

The Farm Bill energy programs have produced a high rate of return for American taxpayers, in terms of viable projects funded and operating and new employment opportunities in rural areas. We will work with Representative Kaptur and other Members of Congress to ensure that these successful programs continue to work.

About BIO

BIO represents more than 1,100 biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology products. BIO also produces the BIO International Convention, the worlds largest gathering of the biotechnology industry, along with industry-leading investor and partnering meetings held around the world. BIO produces BIOtech NOW, an online portal and monthly newsletter chronicling innovations transforming our world. Subscribe to BIOtech NOW.

Upcoming BIO Events 2012 BIO International Convention June 18-21, 2012 Boston, MA

BIO Business Forum June 18 21, 2012 Boston, MA

BIO India International Conference September 12 13, 2012 Mumbai, India

Livestock Biotech Summit September 19 21, 2012 Kansas City, MO

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BIO Applauds Rep. Kaptur’s Energy Investment Act of 2012

CORRECTING and REPLACING Ten U.S. High School Students Win Biotechnology Research Competition

BOSTON--(BUSINESS WIRE)--

In the list of U.S. National BioGENEius Challenge winners, Megan Smith is from Lenexa, Kan. not Lenexa, Ky.

The corrected release reads:

TEN U.S. HIGH SCHOOL STUDENTS WIN BIOTECHNOLOGY RESEARCH COMPETITION

Ten of the brightest young minds in biotech have won the U.S. National BioGENEius Challenge. The winners will now advance to compete with students from Canada and Australia in the International BioGENEius Challenge, which will take place at the 2012 Biotechnology Industry Organization (BIO) International Convention here in Boston. Winners of the International BioGENEius Challenge will be announced tomorrow at the keynote luncheon at the BIO International Convention.

The U.S. National and International BioGENEius Challenges are competitions for high school students who demonstrate an exemplary understanding of biotechnology through science research projects.

U.S. National BioGENEius Challenge winners are:

Julia Abelsky, Sandy Springs, Ga. for her research on Analysis of Cylindrically Confined Diblock Copolymers and Gold Nanocomposites for Metamaterials; Aprotim Bhowmik, Lilburn, Ga. for his research on Arterial Hemodynamics in Atherosclerosis Patients - A Mathematical Model; Nikhil Buduma, San Jose, Ca. for his research on Pertussis Toxin-Mediated Inhibition of Lymphocyte Trafficking into Lung Tissue: Considerations for an Improved Whooping Cough Vaccine; Nidhi Gandhi, Sherwood, Ark. for her research on Phase II: Improving the Effectiveness of Anticancer Drugs with Cell Death Modulators; Nathan Kondamuri, Dyer, Ind. for his research on A Novel Porphyrin Based Solar Cell Combining Coordinated Metal Ion Substitution and Self-Assembly to Broaden the Absorption Spectrum to Efficiently Create Sustainable Electrical Energy; Natalie Ng, Cupertino, Ca. for her research on Interrogation of Cancer: Development of a Novel Biomarker Discovery Tool to Identify Clinical Signatures from Statistically Deconvoluted Expressions; Kevin Nguyen, Plano, Texas for his research on The Development of Novel Sutures that Store and Deliver Nitric Oxide for Wound Healing; Aishwarya Raja, Ramsey, N.J. for her research on Spicing Up the Caspase Pathways: Novel Targeted Curcumin-Loaded Nanoparticles for Alzheimer's Treatment; Morgan Sinko, San Antonio, Texas for his research on Pop Goes the Diesel: A Linoleic Acid/R. rhodochrous Mixture as a Bioremediation Agent of Diesel Contaminants in Saltwater and Freshwater Environments; Megan Smith, Lenexa, Kan. for her research on The Effect of Coffee Extract & Caffeine on the Locomotory Rate and Basal Slowing Response of a LRRK2 Transgenic Caenorhabditis elegans (G2019S Mutation) Model of Parkinson's disease.

The U.S. National BioGENEius Challenge is like the Olympic trials for life science, promoting excellence, curiosity and a biotech-driven career among its participants and these ten students get a chance to compete for gold in the International BioGENEius Challenge, said Tom Wiggans, chairman of the Biotechnology Institute. We encourage our students to understand and make the connection between their research for the vast potential for solving human health, food and environmental problems.

Students were evaluated on the quality of their research and display, their responses to questions relating to their scientific knowledge, and the potential commercial applications of their research.

Original post:
CORRECTING and REPLACING Ten U.S. High School Students Win Biotechnology Research Competition

New Report Finds Biotechnology Companies are Participating in 39% of All Projects in Development for New Medicines and …

WASHINGTON--(BUSINESS WIRE)--

Small- to medium-sized biotechnology companies are bringing innovation to global health, according to a report published today by BIO Ventures for Global Health (BVGH) and the Biotechnology Industry Organization (BIO). The report shows that 134 biotechnology companies are participating in neglected disease research and development, which represents participation in 39% of the 191 new drugs, vaccines, and diagnostics in development for neglected diseases such as malaria, tuberculosis, dengue fever, and others.

Partnering is an important driver for todays biotechnology companies. The new report, Biotechnology: Bringing Innovation to Neglected Disease Research and Development, finds that 64% of all products in development by biotechnology companies across the pipeline of drugs, vaccines, and diagnostics for neglected diseases involve partnering.

According to the report, product development partnerships (PDPs) a unique public-private partnering mechanism created to increase biopharmaceutical participation in neglected disease R&D, government agencies, and academic institutions are driving this biotechnology company partnering for neglected diseases. Although PDPs are the focal point of industry engagement in global health, they are the second most frequent partner to biotechnology companies after academia with involvement in 52% of partnered projects. When a PDP is not involved in a project, biotechnology partnerships with government agencies increase, especially for vaccines and diagnostics.

Across all neglected diseases, biotechnology companies work alone 36% of the time, according to the report. For tuberculosis and dengue fever, companies more frequently overcome barriers and leverage some market potential to work alone. This may be because small to medium-sized companies perceive a potential market opportunity.

We were very pleased to see the level of the biotechnology sectors engagement in global health research and development, as a critical source of innovation. To continue progress in addressing the unmet medical needs of the developing world, both biotechnology companies and global health groups should ramp up commitment and involvement, says Don Joseph, CEO of BVGH. Our new report provides specific recommendations both to biotechnology companies and neglected disease stakeholders from academia, governments, nonprofits, and foundations to increase and improve their collaborative work in neglected disease research. Accelerating solutions for these devastating diseases presents major challenges but can happen if these groups continue and increase their work together.

While the report finds that small to medium-sized biotechnology companies are involved in 39% of all projects for neglected disease, BIO estimates there are nearly 3,000 public and private biotechnology companies worldwide. At least 90% of these companies focus on health research and development, suggesting that the 134 biotechnology companies participating in neglected disease research and development identified in the report represent about 5% of global biotechnology companies.

It is encouraging that small- to medium-sized biotechnology companies that lead the charge in developing life-saving medicines and technologies in the developed world are so engaged in creating new drugs, vaccines, and diagnostics for the neglected diseases primarily affecting the poor in the developing world, says Jim Greenwood, President and CEO of BIO. The true value of this weeks BIO International Convention is to bring together industry leaders who can share insights and engage in discussions focused on potential collaborations that could lead to scientific breakthroughs that will address these and other global challenges.

More than 1.4 billion people are affected by neglected diseases the majority of those affected are poor and living in developing countries. When the term neglected is applied to a disease, it can carry a wide range of implications. Neglected can describe the patient population affected by the disease, the scientific effort underway to understand the disease, or the extent to which new products to prevent, diagnose, and treat a disease are being pursued. Neglected can also describe a health disparity where drugs, vaccines, or diagnostics are available and in use in wealthier or developed countries, but these technologies have not been extended to poorer countries due to challenges of cost, feasibility, or political will.

The BIO International Convention will bring together global biotechnology and pharmaceutical leaders to discuss partnering and collaborations that are focused on moving innovation forward, including scientific breakthroughs for neglected diseases that will have a global impact. More than 15,500 industry leaders will attend the Convention, including companies and advocacy organizations that are focused on finding cures and treatments for tuberculosis, malaria, and dengue fever, among others. More information on the BIO International Convention can be found at http://convention.bio.org.

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New Report Finds Biotechnology Companies are Participating in 39% of All Projects in Development for New Medicines and ...