The Chinese market for drugs and medical devices is increasing fast – and the CFDA (currently, National Medical Products Administration, NMPA) must ensure that any foreign company exporting medicinal products to China complies with the CFDA drug and medical device regulations and standards!
The CFDA’s 2017 Drug Inspection Report indicated the CFDA performed 51 planned inspections in Europe. (http://www.cfdi.org.cn/resource/news/2017pdf_en.html), increased from 33 planned inspections in Europe in 2016. Pharmaceutical and medical device firms exporting products to China have seen a rapid expansion of CFDA overseas inspection in number and expectation on GMP compliance. A CFDA Official announced early this year that the CFDA intended to orderly expand its overseas inspection programs and would further increase the number and intensity of overseas inspections in the coming years. During this Seminar you will get the opportunity to hear from an expert in the field about the CFDA organization and regulatory authority, the CFDA inspection process and strategy, how to interact with the CFDA inspectors, and recommendations to prepare for a successful CFDA inspection. In addition, you will also hear from Industry colleagues about their CFDA inspection experiences.
CFDA Organization & Authority
Qualification of CFDA Inspectors
Inspection Logistics, Formalities and Courtesy
CFDA Inspection Process
Review of Unique CFDA GMP requirements
CFDA Foreign Inspection Focus
Current CFDA Foreign Inspection Trends & Statistics
This course provides the attendees with the essential information and recommendations to promote the preparation for, and to facilitate, a successful CFDA inspection and to avoid CFDA inspection pitfalls associated with cultural diversity.
Personnel within Pharmaceutical or Medical Device/IVD companies who are responsible for handling and/or participating in inspections from authorities, either in companies already selling to the Chinese market or those in the process of getting their products approved and where an inspection may take place in the future. Quality Assurance, GMP compliance and regulatory affairs professionals should also attend to gain the necessary information and knowledge to prepare for a successful CFDA inspection.
In the report, CFDA gives information about both domestic and overseas inspections and you can find examples of their findings as well. Overseas inspections covered 51 enterprises (mainly in Europe and North America) during 2017, a slight decrease compared to 2016. 9 of these inspections didn’t pass and the two major areas where defects were found was QA/QC and Document controls.
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