China GMP and Registration of APIs - Live Online Training

Thursday, 2 November 2023 13.00 - 16.30 h

Course No 20624

All times mentioned are CET.

Our Service

Costs

*ECA-Member:**	EUR 590,--
*Regular Fee:**	EUR 690,--
*EU/GMP Inspectorates:**	EUR 590,--
*APIC Member Discount:**	EUR 640,--

(All prices excl. VAT). Important notes on sales tax.

Registration

* also payable by credit card

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@gmp-compliance.org

Speakers

Marieke van Dalen, Global Regulatory Specialist, Aspen Oss, The Netherlands
Francois Vandeweyer, Freelance Consultant, Belgium, formerly Janssen Pharmaceuticals
Ellen Zandvoort, Aspen Oss, Customer & Regulatory Support Officer, The Netherlands

Objectives

China first introduced GMP in 1988, and since then the GMP regulations are revised and updated several times. Most of the existing GMP requirements and guidance documents were updated by the so called National Medical Products Administration (NMPA), China’s new Drug Regulatory Authority since 2018, and replace former Guidelines published by the CFDA (China Food and Drug Administration). In 2021, the NMPA published a new guideline in regard on the inspection system and GMP certificates, which influenced the certification procedure tremendously.

Also in 2021, the NMPA issued new guidelines with information relevant for changes in registrations of drug products, for administrative and for technical processes. To keep track with the mandatory guidance documents of the regulatory authority as well as the understanding of the GMP requirements and registration procedures for APIs are the prerequisites to register APIs in China.

This Live Online Training provides an overview of the regulatory and GMP requirements regarding APIs in China.

Target Group

This Live Online Training has been developed for all who are dealing with API Sourcing, Manufacturing, Quality Assurance and Regulatory Affairs.

Technical Requirements

We use WebEx for our live online training courses and webinars. At https://www.gmp-compliance.org/training/online-training-technical-information you will find all the information you need to participate in our trainings and you can check if your system meets the necessary requirements to participate. If the installation of browser extensions is not possible due to your rights in the IT system, please contact your IT department. WebEx is a standard nowadays and the necessary installation is fast and easy.

Programme

API Registrations in China
Marieke van Dalen

Health authorities in China
The Chinese Drug Master File System
Bundled review
Specifics for the Chinese API Drug Master File
Common deficiencies

QC Testing: a China Specific Requirement
Ellen Zandvoort

The procedure for QC testing
Common observed hurdles with QC testing

China's Current View on Drug GMP
Francois Vandeweyer

Chinese GMP – general Topics
Chinese Drug GMP – on site inspection focus Points
Chinese GMP annexes with focus on Biologicals and the new Annex 13 for IMPs
Chinese quality management and equipment strategy to compete with the West

Take advantage of the experiences of our speakers and send us your questions related to China GMP and registration of APIs in China prior to the Live Online Training. Your questions are welcome and will be answered as comprehensively as possible by the experts during the Q&A sessions.

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