Pursuant to the new Vaccine Administration Law and the revised Drug Administration Law, the Provisions for Lot Release of Biological Products was revised by the State Administration for Market Regulation, with the aim of ensuring product quality and supply. The provisions will be implemented from March 1, 2021.
The Provisions has eight chapters and 48 articles, and the main amendments include:
Next steps, the National Medical Products Administration (NMPA) will formulate supporting documents to ensure that the various regulations are implemented and ensure that biological products such as vaccines are safe and effective.
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