Management requirements for drug record and data-Trial

On July 1, the  National Medical Product Administration-NMPA issued the requirements for drug record and data management (for Trial), which put forward the principle requirements for the record and data management of drug development, production, operation and use activities, which was formally implemented from December 1. The management requirements are in accordance with the relevant laws and regulations of the drug administration law and the vaccine administration act, and with reference to “the definition of data reliability and industry guiding principles” issued by the United Kingdom in 2015, and the “data reliability and compliance with current drug production quality specificationsRead More →

Thank you for your interests/registration! For complete and full access to our platform, please contact us to subscribe as a paid-up member. The annual fee is CNY 10,000 Best! Paolo yue Email: yuefeng7832@hotmail.com Cell: 008613501397114

Existing Users Log In
   
New User Registration
*Required field