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FDA registration of chemical raw materials, various types of preparation products (oral preparations, external preparations, sterile preparations, biological products, etc.), OTC, plant extracts, foods, health foods, food additives, food contact substances, medical devices, etc. Including DMF, ANDA, NDA, IND and other documents; NDC number, PIN number applications, FCN registration, etc.; BE, clinical trials, product testing implementation.

 

CE certification for chemical raw materials, plant extracts, and various types of preparations (oral preparations, sterile preparations, etc.).

Key pharmaceutical intermediates customer audit related matters refer to GMP-management

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