ChemWerth "cGMP In A Changing World" 2008 Seminar
In November 2008, ChemWerth held a cGMP training seminar to coincide with the 2008 API China exhibition held in Suzhou China. The ChemWerth seminar theme was “cGMP In A Changing World”. With 85 “students” from approximately 30 of ChemWerth’s cooperating partner factories throughout all parts of China in attendance, the seminar attendees reported it to be a great success.
To achieve success in the pharmaceutical manufacturing business, it is imperative that manufacturers continuously update their knowledge, train staff, and enforce cGMP compliance as everyday standard practice. Maintaining cGMP compliance is a continuously advancing and challenging requirement for any manufacturer in the pharmaceutical industry. Factories that passed an inspection over the prior ten years, may no longer be prepared to pass today’s rigorous standards. It is no longer only the USA FDA and EU authorities who require regulatory and cGMP compliance for export products. Today, China’s SFDA has taken an active role in demanding strict compliance standards for non-export product as well.
ChemWerth’s Suzhou cGMP training seminar included respected expert speakers from SFDA and FDA, including Mr. Zhong Guangde - SFDA, and aseptic (sterile) process expert Mr. Jerry Shi, all of whom provided updated standards guidance and valuable training to our attendees. In addition, ChemWerth’s own in-house experts, Executive Vice President Song Lin, Dr. Tangsheng Peng, Director of Regulatory and cGMP Compliance, Whenchu Hu, CW China Regulatory-cGMP advisor, and Zhijian Yin, CW China R & D Director, also provided presentations on current hot topics on FDA and ICH guidelines to the factory attendees.
Today, if you cannot pass an inspection, you will lose sales. ChemWerth’s partner factories in China enjoy an advantage that can keep them ahead of the growing and fierce competition in API supply. Unlike most API sales partners, ChemWerth can provide ongoing training and guidance through our educational seminars, continuous support and on-site audits that mirror those of regulatory agencies, and our expert knowledge and support throughout the R & D, DMF filing, and cGMP inspection processes. With ChemWerth, it is a Win-Win situation for all.
ChemWerth understands the importance of maintaining continuous cGMP compliance for your success. For nearly 30 years, our expertise and support has contributed to the development and improvement of China’s professional staff knowledge and API manufacturer’s success. Our seminars are just one way we provide valuable advantage and advancement to our cooperating partner factories. This seminar not only provided a cGMP knowledge feast to all factories, but also built a communication bridge for all the cooperating factories to know each other well. We believe ChemWerth can do more to contribute to your future success!
Please contact ChemWerth if you would like more information on our Regulatory, cGMP or Product Development seminars.
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