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GOOD MANUFACTURING PRACTICES FOR …
Working document September 2009 RESTRICTED GOOD MANUFACTURING PRACTICES FOR pharmaceutical PRODUCTS containing hazardous SUBSTANCES DRAFT FOR COMMENT World Health Organization 2009 All rights reserved. This draft is intended for a restricted audience only, the individuals and organizations having received this draft. The draft may not be reviewed, abstracted, quoted, reproduced, transmitted, distributed, translated or adapted, in part or in whole, in any form or by any means outside these individuals and organizations (including the organizations' concerned staff and member organizations) without the permission of the World Health Organization. The draft should not be displayed on any web site. Please send any request for permission to: Dr Sabine Kopp, Quality Assurance Programme, Quality Assurance & Safety: Medicines, Department of Essential Medicines and pharmaceutical Policies, World Health Organization, CH-1211 Geneva 27, Switzerland.
working document qas/08.256 rev.1 september 2009 restricted good manufacturing practices for pharmaceutical products containing hazardous substances
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