To help companies evaluate their strategies for pharmaceutical regulatory management from the complex regulations and policies, clinical research, GMP technical requirements, and post-marketing supervision we developed the “Training Series for Pharmaceutical Process Management”. These training series focus on several important circulation links to drug research and development, clinical, production, quality and sales. It systematically and comprehensively sort out and interpret regulatory requirements, basic knowledge, verification points and supervision focus of drug management. Also, with case study and effective interaction, the switch from knowledge to practice is shortened and the training effect is better ensured.

BaiPharm has formed a set of relatively mature and complete training courses, which mainly cover the following:

    Regulatory affairs guidance and best pathways to China

    Product registration (NDAs, ANDAs & MA + MAH)

Drug Master File (DMF) filing

    GMP compliance and certification

    market regulatory supervision of drugs

For course needs not found on the above course list, please feel free to email us at info@baipharm.com with the subject “Supplementary Course”, explain your course requirements (including the required course content, time, number of trainees, etc.). Be sure to leave detailed contact information (including name, work unit, position, contact address, zip code, telephone, etc.) for the Expert Team to directly reach out with the relevant information and course details.