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Bayer and Onyx Initiate Nexavar Trial: Bayer HealthCare and Onyx Pharmaceuticals have begun enrolling patients in a Phase III trial in order to evaluate Nexavar tablets in combination with oral chemotherapeutic capecitabine. The trial was started based on positive results from a group-sponsored Phase II trial that ...

FDA Takes Action to Remove Unapproved Drugs from US Market: The US Food and Drug Administration (FDA) has initiated action against companies that manufacture, distribute or market certain unapproved prescription oral cough, cold, and allergy products. Unapproved prescription products have not been evaluated by the FDA for safety, ...

Product Animations Offers Customized, Computer Animated Virtual Training for Processing and Packaging Equipment Operations: Studies Show that Approach is Five Times More Effective for Training Product Animations, Inc. (PAI) a leading provider of custom, computer-based virtual training and reference programs for manufacturing and packaging equipment, offers customized animated training programs to ...

Evonik finalizes acquisition of Boehringer Ingelheim s RESOMER business: Extending its technology base to increase value creation and boost growth Strengthening its position as a strategic partner to the pharmaceuticals industry Evonik Industries formally acquired the entire RESOMER business of Boehringer Ingelheim Pharma GmbH & Co. KG on March 1,2011...

SFDA held videoconference on carrying out Good Manufacturing Practice for Pharmaceutical Products (2010 revised edition): On February 25, 2011, the State Food and Drug Administration (SFDA) held a videoconference on carrying out Good Manufacturing Practice for Pharmaceutical Products (2010 revised edition) (hereinafter referred to as the new version of GMP). The conference introduced the significanc...

Three Day Excipient GMP Auditing Workshop- Arlington VA: Tuesday April 5-Thursday April 7, 2011 Three day Workshop Content A comprehensive workshop in excipient auditing for makers and users. Training will analyze the essential elements of excipient good manufacturing practice for materials intended for use in pharmaceuticals or ...

Study shows lower success rate of FDA drug approval from 2003 to 2010: Biotechnology Industry Organization (BIO) Industry Analysis and BioMedTracker (BMT) announced results of a study today that shows the overall success rate for drugs moving through clinical trials to FDA approval from late 2003 to the end of 2010 is near one in 10. Previous ...

Sanofi-aventis, Sunnybrook enter agreement to develop and commercialize vasculotide: Sanofi-aventis (EURONEXT: SAN and NYSE: SNY) and Sunnybrook Health Sciences Centre (Toronto, Canada) announced that they have entered into a research agreement and licensing option for vasculotide, an investigational compound to treat chronic wounds. This includes neuropathic ...

Cancer Drug Used in Combination with Other Therapies Associated With Increased Risk of Death: [object Object]

FDA Funding to Rise: The US Food and Drug Administration (FDA) budget is set to rise by $147m to $2.7bn under President Obama's 2012 budget proposal. The agency is also set to receive approximately $1.6bn in fees paid by pharmaceutical, medical device and tobacco companies, equating to a total budget ...

GAO Report Faults FDA s Response to Heparin Crisis: Agency s use of outside experts violated ethics rules Although the U.S. Food and Drug Administration s (FDA) response to the contamination of heparin sodium in 2008 helped protect the public health, the agency violated government-wide ethics standards in doing so, stated a report ...

UK Takes U-Turn on Chinese Medicine Ban: The UK Government will allow several unlicensed herbal and Chinese medicines to escape a proposed European ban, which was due to go ahead in April. The controversial move will see health food shops continue to stock pills and supplements such as cascara black, used as a laxative ...

Good Manufacturing Practice for Pharmaceutical Products (2010 revised edition) issued: The Good Manufacturing Practice for Pharmaceutical Products (2010 revised edition) (hereinafter referred to as the new version of GMP) was recently issued and will come into effect as of March 1, 2011, after five years of amendments and two rounds of public consultation. Since ...

Sheffield Bio-Science forms strategic alliance with Wockhardt to strengthen cell culture media portfolio: Sheffield Bio-Science, a Kerry Group Business, has formed a strategic global sales, marketing and development alliance with Wockhardt Ltd. Under this partnership, Sheffield Bio-Science will be the Exclusive Global Sales and Distribution Partner for recombinant insulin manufacture...

Takeda submits NDA to FDA for fixed-dose combination of azilsartan medoxomil plus CLD to treat hypertension: Takeda Pharmaceutical Company Limited (Takeda) announced today that Takeda Global Research & Development Center, Inc. U.S., submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for an investigational fixed-dose combination of azilsartan medoxomil ...

ExcipientFest Americas: May 10 - 11, 2011 - Renaissance Harborplace Hotel, Baltimore, MD Pharma Industry's BEST Event for Regulatory, Science and Sourcing Education ExcipientFest attracts Pharmaceutical Scientists from the Americas and around the world to a unique two day forum for cutting-edge ...

US Congressmen Vows to Fight for Drug Market Competition: US Congressman Henry Waxman has vowed to fight to promote competition within the pharmaceutical industry, adding that the US Food and Drug Administration's 32-month approval time for generic drugs is "inexcusable". Speaking at the World Generic Medicines Congress in London, UK, ...

CPhI Worldwide 2011: We are delighted to announce the official opening of CPhI Worldwide 2011, taking place at Messe Frankfurt, Germany, from 25 27 October. With a substantial global visitor audience, a tailored conference programme and an expanding range of co-located events, CPhI offers you the ...

Avastin debate spills over until June FDA hearing: By Dr Ananya Mandal, MD The U.S. Food and Drug Administration have granted Roche a hearing in June to defend the cancer treatment Avastin. The hearing would examine the effectiveness of the drug in breast cancer. FDA s oncologic drugs advisory committee would hear the arguments. ...

EvaluatePharma data shows poor R&D productivity measures both in quality, quantity: Pharmaceutical R&D productivity is consistently undercounted. Most reports fail to fully count the number of new drugs that reach the market, missing out on billions of dollars of sales generated by R&D investment, an analysis of EvaluatePharma data shows. Most counts of FDA new ...

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Bill Gates talks nuclear: Microsoft co-founder Bill Gates confirmed on Wednesday that he is ...

China offers inspirations to global dilemmas: BEIJING, Jan. 22 (Xinhua) -- Policies of China's new leadership in the ...

Merck to put $1.5b in R&D: Merck Sharp & Dohme (MSD), the world's second-largest drug producer by ...

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IMF chief warns of risks to recovery: DAVOS, Switzerland, Jan. 25 (Xinhua) -- The International Monetary ...

China's farm product pricing plan shifts to market orientation: The Number One Document also proposed a new pricing plan for China's ...

Chinese investors look to overseas opportunities: SHANGHAI, Jan. 25 (Xinhua) -- China, the world's top manufacturer and ...

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Retailer's Net Profit Falls 3%: A Wal-Mart store is seen in Stratford, Connecticut, the United States. ...

Gaming Firms Find Going Tough: Employees demonstrate Sony Ericsson Mobile Communications' Xperia Play ...

Boeing Wins Biggest Order of US$26b: A formation of nine Royal Air Force Red Arrows Hawk aircraft fly ...

trade

sports

Yao's gift of sport for all: Chinese NBA player Yao Ming teaches a boy with special needs how to ...

Lucrative golf industry lures stiff competition: Two models stand beside golf equipment and bags at a recent golf ...

Li Na wins French Open women's singles title: History-making tennis legend Li Na notched the first-ever grand slam ...

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