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Last updated on April 18, 2014 at 1:21 EDT

Latest State Food and Drug Administration Stories

2013-08-27 08:28:07

-- MDiT Forum and Regulation Summit adds substantial value to Asia's pre-eminent medical device manufacturing exhibition -- SHANGHAI, Aug. 27, 2013 /PRNewswire/ -- MEDTEC China 2013 would not be the same without its traditional co-located on-site conference and once again this year, it welcomes a top-class event: the MDiT Forum and Regulation Summit 2013. The organizers are happy to announce that the schedule is now very close to being finalized. The three-day multi-module event...

2013-03-27 08:31:54

SHANGHAI, March 27, 2013 /PRNewswire/ -- Life Technologies Corporation (NASDAQ: LIFE) today announced that its Applied Biosystems 3500xL Dx Genetic Analyzer has been approved by China's State Food and Drug Administration (SFDA) for clinical diagnostic use in China and the launch of 10 Assays from its joint venture with Daan Gene. The development marks a major extension of Life Technologies' capabilities to serve the clinical end market in China with Sanger-based solutions. The 3500xL Dx...

2013-01-28 08:28:47

JERSEY CITY, N.J., Jan. 28, 2013 /PRNewswire/ -- Aoxing Pharmaceutical Company, Inc. (NYSE MKT: AXN) ("Aoxing Pharma"), a specialty pharmaceutical company focusing on research, development, manufacturing, and distribution of narcotic, pain-management, and addiction treatment pharmaceuticals, today announced that its Chinese subsidiary has received from the State Food and Drug Administration of China ("SFDA") a license to produce the active pharmaceutical ingredient ("API") in Pholcodine....

2013-01-07 08:28:31

ROCKVILLE, Md., Jan. 7, 2013 /PRNewswire/ -- EntreMed, Inc. (Nasdaq: ENMD), a clinical-stage pharmaceutical company developing therapeutics for the treatment of cancer, announced today that EntreMed has submitted a new drug clinical trial application with China's State Food and Drug Administration (SFDA) for its proprietary drug candidate, ENMD-2076, to conduct global clinical trials in triple-negative breast cancer patients. (Logo: http://photos.prnewswire.com/prnh/20010620/ENMDLOGO )...

2012-09-11 02:28:58

BEIJING, Sept. 11, 2012 /PRNewswire-FirstCall/ -- Dehaier Medical Systems Ltd. (NASDAQ: DHRM) ("Dehaier"), an emerging leader in the development, assembly, marketing and sale of medical devices and homecare medical products in China, today announced that it has obtained State Food and Drug Administration approval for DHR-CPAP-C5, one of Dehaier's major proprietary homecare medical devices. The period of validity for the SFDA approval is four years. (Logo:...

2012-08-16 02:24:36

SHANGHAI, Aug. 16, 2012 /PRNewswire-Asia/ -- WuXi PharmaTech (NYSE: WX) today announced that its toxicology facility in Suzhou had received a Certificate of Good Laboratory Practice (GLP) from the State Food and Drug Administration (SFDA) of the People's Republic of China after successfully passing two GLP inspections conducted by the SFDA. Good Laboratory Practice is a quality system concerned with the organizational processes and conditions under which health safety studies are...

2012-08-03 14:22:49

XIANYANG, China, Aug. 3, 2012 /PRNewswire-Asia/ -- Biostar Pharmaceuticals, Inc. (NASDAQ GM: BSPM) ("Biostar" or "the Company"), a PRC-based manufacturer and marketer of pharmaceutical and health supplement products in China for a variety of diseases and conditions, today announced that on July 30, 2012, after a thorough inspection of raw materials used in every production category, it received "green-light" approval from Xianyang State Food and Drug Administration (SFDA) authorities to...

2012-06-11 02:25:25

BEIJING, June 11, 2012 /PRNewswire-Asia/ -- Sinovac Biotech Ltd. (Nasdaq: SVA), a leading provider of biopharmaceutical products in China, today announced a positive SFDA inspection of the three clinical trial sites being used in the Company's Phase III study of its proprietary inactivated Enterovirus 71 (EV71) vaccine against hand, foot and mouth disease (HFMD). In May 2012, an expert from the Center for Drug Evaluation within the State Food and Drug Administration (SFDA) completed an...

2012-05-30 10:25:31

XIANYANG, China, May 30, 2012 /PRNewswire-Asia/ -- Biostar Pharmaceuticals, Inc. (NASDAQ GM: BSPM) ("Biostar" or "the Company"), a PRC-based manufacturer and marketer of pharmaceutical and health supplement products in China for a variety of diseases and conditions, today announced that, following an onsite inspection by Xianyang's State Food and Drug Administration (SFDA), samples from a batch of its Xin Aoxing capsules were found to contain a chromium content higher than edible...

2012-04-19 18:20:19

NEWARK, N.J., April 19, 2012 /PRNewswire-Asia-FirstCall/ -- American Oriental Bioengineering, Inc. (NYSE: AOB), (the "Company" or "AOB"), a pharmaceutical company dedicated to improving health through the development, manufacture and commercialization of a broad range of prescription and over-the-counter ("OTC") products, today announced that four out of its five manufacturing subsidiaries are undergoing onsite short notice inspections directed by China State Food and Drug...