China DMF Filing Webinar

Accestra Webinars

In collaboration with Pharma To Market, we invite you to join us for a complimentary webinar on 24 October 2024.

Mastering Registration of Drug Master File (DMF) in China
for APIs, Excipients & Packaging Materials

Are you navigating the complexities of Drug Master File (DMF) registration in China? Join us for an exclusive webinar where we’ll dive into the essential strategies and regulatory pathways to ensure a successful DMF submission.

Key Topics Covered:

• China DMF Regulatory Framework – Gain a comprehensive understanding of China’s evolving regulatory landscape.
• China DMF Pathways – Learn the critical steps for streamlining your submission process.
• Comparison of Global DMF Standards – See how China’s DMF process compares to the US DMF, EU CEP, and ASMF.
• Timelines and Requirements – Get a clear roadmap of what to expect in terms of documentation and timing.
• Tips & Pitfalls – Hear expert advice on common challenges and how to avoid costly delays.

Who Should Attend:

This webinar is designed for regulatory affairs professionals, pharmaceutical companies, and international businesses involved in China DMF registration or looking to expand into the Chinese market.

Date:

24 April 2024, Thursday

Time:
15:00 – 16:00 China/Singapore/Malaysia

17:00 – 18:00 Sydney

05:00 – 06:00 EST

09:00 – 10:00 CET

03:00 – 04:00 EDT