USP 711 Dissolution sickness policy

USP 711 Dissolution sickness policySOP 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

and under pressure as needed

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

together with their purchase and acceptance

These must be followed and documented at the time of performance

any retrieval of them from the distribution network should be regarded and managed as recall

You must establish a specification for identity

and from accredited sources

identification

and furnish running water that is safe and sanitary at a suitable temperature

water supplies

For the production of dietary supplements you must use equipment and utensils that are of appropriate design

or examination by the quality control unit before release for manufacturing