EU GMP Annex 1: Manufacture of Sterile Medicinal Productshas been published.

Written By Nigel Slater

What is Annex 1?

Annex 1 of the EU GMP (Good Manufacturing Process) guidelines describes the European Union’s requirements for the manufacture of sterile medicinal products, including those imported from non-member nations. The latest revision, recently released, is expected to have a greater reaching impact on QA/QC and all laboratory activities.

CM Supply’s selection of new products include:

NEW high filtration antimicrobial cleanroom fabrics

NEW technical garment design to work with our new high filtration fabrics

NEW hood design to work with our cleanroom goggles

NEW socks – pre-processed to ISO5

“It has taken a decade to get to this point and there is only one year before it takes effect. At CM Supply we have been anticipating this and have cleanroom garments and consumables ready to supply.”

— Nigel Slater, CEO, CM Supply Limited

Nigel Slater
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