Cisema Webinar on Drug Registration Pathways in China

Cisema Webinar on Drug Registration Pathways will provide an overview of the regulatory environment for medicines in China, including regulatory authorization pathways. The webinar will be hosted by The Organisation for Professionals in Regulatory Affairs (TOPRA) on April 26, 2022.

April 26, 2022 | 9:30 GMT | Cisema Webinar on Drug Registration Pathways in China

Learning objectives

By engagement in this webinar, the delegate will:

Understand approval pathways for drugs approval in China

Be able to explain key milestones, timelines and dossier requirements for China drug approvals

Target Audience

Regulatory professionals in UK and EU who want to familiarise themselves with the Chinese Regulatory environment for medicines

Investors who want to understand more about key requirements for portfolio companies

Presenters

Guo Ning

General Manager Cisema Beijing

Guo Ning is an industry executive with degrees from Nankai University Tianjin (China) and University of Mannheim (Germany) who has developed a deep expertise in China market access issues via his experiences in industry, as a project manager at an import/export business, and as a technical compliance and product safety expert with Cisema for over 15 years.

Hamish King

COO of Cisema Group

Admitted as a lawyer in Hong Kong and in New South Wales, Australia and formerly with Magic Circle firm Linklaters in Hong Kong, Hamish lives in Hong Kong regularly writes and presents on China regulatory affairs life sciences topics.

Contact Cisema if you would like to learn more about the event or register here.