USP 711 Dissolution sickness policy together with their purchase and

together with their purchase and acceptance

or examination by the quality control unit before release for manufacturing

identification

You must establish a specification for identity

Good Manufacturing Practice (GMP) ensures that products are consistently produced and managed to the quality standards appropriate to their intended use and as required by the Marketing Authorisation or product specification

USP 711 Dissolution sickness policy together with their purchase andSOP and report form for tablet or capsule dissolution testing of by Quality Control according to USP <711> and EP 2. 9. 3 including slow or delayed release