SHANGHAI, Sept. 27, 2012 /PRNewswire/ -- Pharma Manufacturing & Quality Management China 2012, organized by CPhI Conferences, will be held on 6th-7th November in Suzhou, China. The event will gather 120+ decision makers from both government institutions and pharmaceutical companies to discuss hot topics including quality management systems, API manufacturing, solid dosage form production and sterile drug products. It will provide an interactive communication platform for professionals in the pharmaceutical industry to benchmark their business and technology against 'best in class' and ensure that they have the tools they need to form a coherent and logical strategy.
High-level Speakers Including:
- Deng Haigen, Senior Engineer /2010 version of GMP Drafting Expert, Sino-Swed Pharmaceutical Corp. Ltd.
Intro: Mr. Deng had been Senior Director of Quality Assurance (QA) for Sino-Swed Pharmaceutical Co., Ltd. for 1 8years. China Pharmaceutical Association of Plant Engineering Senior Professor / Advisor, GMP Editor / translator of the book titled "Guidelines of European GMP"- 2008; "Guidelines of validation on pharmaceutical processing, 2nd revision"- 2003. and "Guidance of GMP Application for Pharmaceutical Industry." Invited by SFDA as a member of working group for Revision of China GMP.
- An Guohong, Quality Director, North China Pharmaceutical Group Corporation
Intro: Ms. An has over 20 years experience in QA, QC, pharmaceutical manufacturing management, quality management in the field of free drying, oral solid dosage, API, sterile drug, etc. She has lead 11 GMP certifications in North China Pharmaceutical Group Corporation.
- David Chen, VP, Quality and Regulatory Affair, Shanghai Desano Chemical Pharmaceutical Co., Ltd
Intro: Dr. David Chen has more than 20 years of pharmaceutical development experience in the areas of process analytical technology, spectroscopy, solid state characterization, chemical process development and GLP/GMP compliance. Dr. Chen served as Manager for Schering-Plough Global Quality and as a Research Leader for Roche Pharmaceuticals in USA before joining Desano.
- Xu Hefeng, Senior Document Manager, Northeast Pharmaceutical Group Import and Export Company
Intro: Mr. Xu has over 20 years experience in international pharmaceutical registration and certification and has in-depth insight of EU/USA regulatory, GMP compliance, labrotary management, verification, risk analysis, etc. He has been involved in compiling and publishing GMP Training tutorials, ICH API Quality Control and The Implementation of APIC-Q7, API Process Verification, etc.
Ms. Tracy Cui
SOURCE CPhI Conferences