April 15-16, 2023, the Second Polypeptide Pharmaceutical Industry Innovation Forum will be held in Buckingham Grand Hotel (Xiangcheng store)，Suzhou City, Jiangsu Province. As an invited guest, gempex is honored to attend this conference. Mr. Andy Chen, theGMPexpert from gempex, will give a talk on the international GMP compliance requirements for the production of polypeptide drugs. Thank you for your attention and invite you to the scene!

Conference information

The theme of the Second Polypeptide Pharmaceutical Industry Innovation Forum is "Focusing on New technologies to build new polypeptides". There are two forums in the conference: one focusing on polypeptide drug development and clinic; the other focusing on polypeptide drug CMC forum. The conference is committed to providing an in-depth platform of thought collision and experience sharing for polypeptide drug experts and researchers. 800 people were expected to attend the meeting.

Conference related information

• Conference Name: 2023 The Second Polypeptide Pharmaceutical Industry Innovation Forum
• Meeting Date: April 15-16, 2023
• Location: Buckingham Grand Hotel, Suzhou, Jiangsu (Xiangcheng Store)
• Sponsor: E Pharmaceutical Academy

Scan the QR code for the detailed schedule and registration information.（Only in Chinese）

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gempex lecturer introduction

• Topic: International GMP Compliance Requirements for the Manufacture of Polypeptide Drugs
• Lecture time: 16:20-17:10, April 16, 2023
• Lecturer: Andy Chen, GMP Expert from gempex China

Andy Chen, GMP Expert

• Mr. Chen executed the development of product analysis methods, qualification and validation and technical transfer in American laboratory; and he was as QC supervisor and QA manager of a large listed company, fully responsible for the compliance of the system, self-inspection of the group company, and participated in the US FDA inspection for many times.
• Mr. Chen is good at drug preparation process and the international compliance analysis laboratory, responsible for quality system management, qualification and validation, computerized system validation, etc. What’s more, he lead and participated in accordance with international GMP related audit, gap analysis and mock inspection for over 15 times