Navigating China’s API Regulations: An Essential Guide to DMF Registration
As China becomes an increasingly important market for pharmaceutical companies, compliance and safety are crucial.
This webinar has been designed to provide participants with a better understanding of the latest developments in China's Active Pharmaceutical Ingredients (APIs) regulations, including the new Drug Master File (DMF) registration routes that protect the confidentiality and interest of active drug substance suppliers.
Join our panel of industry experts as they discuss API registration in China and the quickest pathway options for DMF registration. Gain valuable insights into the related requirements and stay up-to-date with the dynamic and fast-changing regulations in China.
Don't miss this opportunity to enhance your knowledge of DMF, API, and China and learn from our industry leaders from this important region.
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Benefits of Attending
- Gain in-depth knowledge and insights on how to register your Active Pharmaceutical Ingredient (API) in China
- Stay up-to-date on the latest API and DMF regulations and requirements for China
- Enhance your regulatory knowledge and skills for China and learn about the local requirements for Active Pharmaceutical Ingredient (API) registration
- Ensure compliance and safety by staying informed of the latest regulatory developments in China's API registration process
- Engage with industry experts and get your questions answered in real-time
- Gain competitive advantage by understanding the complexities of API registration in China and the quickest and most effective pathways for registration
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About IPI Academy
International Professional & Industry Academy (IPI) is an international leading professional training organisation based in London. Our training solutions provide a return on your investment with measurable results, and are delivered by experienced professionals and managed with exceptional care and...