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Since its creation, pic/s has been active in the development and promotion of harmonised gmp standards and guidance documents C’est ce qui a amené le comité des officiels de la pic à proposer la création du système de coopération en matière d’inspection des produits pharmaceutiques (pic/s). The main instrument for harmonisation has been the pic/s.

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Senior management’s leadership and active participation in the pharmaceutical quality system is essential The main instrument for harmonisation has been the pic/s gmp guide, which pic/s is striving to keep equivalent in terms of gmp requirements with the eu gmp guide, which involves close co. This leadership should ensure the support and commitment of staff at all levels and.

All spanish medicinal authorities, which are listed on the aemps web site, are considered as pic/s participating authorities and are represented in pic/s by the aemps.

If you wish to export to a country whose regulatory authority is a pic/s member, you first need to register your medicinal product with that regulatory authority It’s only once your product has. This guide excludes whole blood and plasma as the pic/s gmp guide for blood establishments lays down the detailed requirements for the collection and testing of blood.