GUIDE TO GOOD MANUFACTURING PRACTICE FOR …

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PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009 8 (Annexes) 15 January 2009 PE 009 8 (Annexes) 15 January 2009 GUIDE TO good MANUFACTURING PRACTICE FOR medicinal PRODUCTS ANNEXES PIC/S January 2009 Reproduction prohibited for commercial purposes. Reproduction for internal use is authorised, provided that the source is acknowledged. Editor: PIC/S Secretariat 14 rue du Roveray CH 1207 Geneva e mail: web site: Table of contents PE 009 8 (Annexes) i 15 January 2009 ANNEXES Annex 1 Manufacture of sterile medicinal 1 1 1 Clean room and clean air device 2 Clean room and clean air device monitoring.

Table of contents PE 009-8 (Annexes) -i-15 January 2009 ANNEXES Annex 1 Manufacture of sterile medicinal products.....1

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