Transcription of SUPPLEMENTARY GUIDELINES ON GOOD …
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SUPPLEMENTARY GUIDELINES ON GOOD …
Working document May 2016 Draft document for comment Draft document for comment SUPPLEMENTARY GUIDELINES ON 1 good manufacturing PRACTICES FOR HEATING, 2 VENTILATION AND AIR-CONDITIONING SYSTEMS FOR 3 NON-STERILE PHARMACEUTICAL DOSAGE FORMS 4 (May 2016) 5 REVISED DRAFT FOR COMMENT 6 7 8 9 10 11 World Health Organization 2016 12 All rights reserved. 13 This draft is intended for a restricted audience only, the individuals and organizations having 14 received this draft. The draft may not be reviewed, abstracted, quoted, reproduced, transmitted, 15 distributed, translated or adapted, in part or in whole, in any form or by any means outside these 16 individuals and organizations (including the organizations' concerned staff and member 17 organizations) without the permission of the World Health Organization. The draft should not be 18 displayed on any website. 19 Please send any request for permission to: 20 Dr Sabine Kopp, Group Lead, Medicines Quality Assurance, Technologies, Standards and Norms, 21 Department of Essential Medicines and Health Products, World Health Organization, CH-1211 22 Geneva 27, Switzerland.
working document qas/15.639/rev.1 page 2 41 schedule for the proposed adoption process of 42 document qas/15.639 43 supplementary guidelines on good manufacturing 44 practices for heating, ventilation and air-
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