NEW YORK, NY--(Marketwire - December 21, 2009) -
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China Aoxing Pharmaceutical Company, Inc. (OTCBB: CAXG) (“China Aoxing”), a pharmaceutical company specializing in research, development, manufacturing and distribution of narcotic and pain-management products, today announced that it has successfully passed the Good Manufacturing Practice (GMP) re-certification of four dosage forms, including capsule, tablet, granule and oral solution formulations, at its new manufacture and packaging facility. The certificate of compliance has a five-year term and was issued by the State Food and Drug Administration (SFDA) following a site inspection.
“Good Manufacturing Practice” is a body of internationally accepted regulations set forth by drug agencies in many countries. GMP compliance ensures that pharmaceuticals, active ingredients and medical devices are produced and quality-controlled according to state-of-the-art standards. According to the National Medicine Administration Law of the People’s Republic of China, all pharmaceutical manufacturers must pass an examination every five years to renew their GMP Certificates.
“We are very pleased to obtain the GMP re-certification of four dosage forms, which is an important milestone in the process of our production facility consolidation,” said Zhenjiang Yue, Chairman and the CEO of China Aoxing. “The re-certification will serve as a critical step to alleviate product backlog associated with these dosage forms. In addition, we expect more GMP re-certification of pill and tincture dosage forms at our brand new product facility in the first half of year 2010.”
About China Aoxing Pharmaceutical Company, Inc.
China Aoxing Pharmaceutical Company, Inc. (OTCBB: CAXG) is a pharmaceutical company located in China specializing in research, development, manufacturing and distribution of a variety of narcotics and pain-management products. Headquartered in Shijiazhuang City, the pharmaceutical capital of China, outside of Beijing, China Aoxing has China’s largest and the most advanced manufacturing facility for highly regulated narcotic medicines, addressing a very under-served and fast-growing market in China. Its facility is one of the few GMP facilities licensed for narcotics medicines. The Company is working closely with the Chinese government and SFDA to assure the strictly regulated availability to medical professionals of its narcotic drugs and pain medicines throughout China.
Statements made in this press release are forward-looking and are made pursuant to the safe harbor provisions of the Securities Litigation Reform Act of 1995. Such statements involve risks and uncertainties that may cause actual results to differ materially from those set forth in these statements. The economic, competitive, governmental, technological and other risk factors identified in the Company’s filings with the Securities and Exchange Commission, including the Form 10-KSB for the year ended June 30, 2008, may cause actual results or events to differ materially from those described in the forward looking statements in this press release. The Company undertakes no obligation to publicly update or revise any forward-looking statements, whether because of new information, future events, or otherwise.
Contact:
Wei Zhang
China Aoxing Pharmaceutical Company, Inc.
Email: chinaaoxing@gmail.com
Telephone: 646-367-1747
Website : www.chinapainmed.com