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SCHEDULE M GOOD MANUFACTURING PRACTICES AND …
www.rajswasthya.nic.ininspection and reference and the manufacturing premises shall be used exclusively for production of drugs and/or no other manufacturing activity shall be undertaken therein except in respect of units licensed prior to 11th December’2001. PART – I Good Manufacturing Practices for Premises and Materials 1. GENERAL REQUIREMENTS --- 1.1.
GUIDANCE ON GOOD DATA AND RECORD MANAGEMENT …
www.who.intinspections regarding data management practices the Committee endorsed the proposal. Following this endorsement, a draft document was prepared by the colleagues from PQT-Inspection and a drafting group, including national inspectors. This draft was discussed at a consultation on data management, bioequivalence, good manufacturing practices and