Ensure access to the Chinese market

NOTE. On hold due to Covid-19

Preparing, Participating and Handling a Chinese Food & Drug Administration (CFDA) Inspection

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!

Course description

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.

Course outline

CFDA Organization & Authority

  • Brief history of CFDA
  • Organization and structure of CFDA
  • CFDA Drug and Device inspection program and procedures
  • CFDA regulatory authority: domestic vs. foreign companies
  • CFDA regulatory actions: domestic vs. foreign companies

Qualification of CFDA Inspectors

  • Education, training and experience requirements
  • Command of English language
  • Training programs available to, and/or provided to CFDA inspectors
  • Qualification requirements to perform foreign inspections
  • Comparison with FDA & EU inspectors

Inspection Logistics, Formalities and Courtesy

  • Provide or offer assistance for travel arrangements; e.g., hotels, ground transportation
  • Proper reception of CFDA inspectors
  • Meals and entertainment for CFDA inspectors
  • Use of interpreters
  • Translation of documents

CFDA Inspection Process

  • Inspection scheduling and planning (length of inspection, number of inspectors)
  • Preparing responses and documents to standard administrative questions or requests
  • CFDA inspection techniques (e.g., walk-through inspection, follow path of drug and medical device production, etc.)

Review of Unique CFDA GMP requirements

  • Comparison with US and EU GMP requirements

CFDA Foreign Inspection Focus

  • Examples: data integrity, consistent actual manufacturing and control practice with submitted or approved applications, laboratory controls with Chinese Pharmacopeia and other technical standards

Current CFDA Foreign Inspection Trends & Statistics

  • Statistics and trends over the years
  • Examples of CFDA issued citations

Learning objectives

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.

Who should attend

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.

CFDA (Chinese FDA) Inspection report for 2017


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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Date & Time
December 8, 2020
- December 8, 2020
ON-HOLD 09.00-17.00 CET
IndustryMedical Device, Pharmaceuticals
LanguageEnglish
LevelAdvanced, Intermediate
LocationAmsterdam
RegionEU

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In-House Training

This course is available as an In-House Training course. Let us know if you wish to customize a course or if you are a large group with the same requirements.

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Your Instructor(s)

Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.

Daniel Stenströmer

Mel Dong

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