courses • Good Manufacturing Practice {Schedule-M} • Good Laboratory Practice {Schedule-L-1} • Documentation Management System • Quality Program Preparation & Audit.• Industrial Microbiology & Sterilization • Clean Room Concept : HVAC• Validation & Stabilities Studies.Client –Site Programmer • In-house training • Internal audit• Human resource development • Facility assessment for cGMPGuidance –• New Manufacturing set-up ,• Existing premises: Extension, Modification.• Documentation –• Dossiers in CTD format & Drug Master File (DMF).• Validation & stability studies, Vendor selection.• Utility system: HVAC, Water system, compressed air.Certifications- WHO-GMP,National Agency of Food Drug Administration & Control NAFDAC-Nigeria. Tanzania Food & Drug Administration-TFDA-Tanzania , National Drug Authority-NDA-Uganda. HSA-Health Science Authority-Canada. Mexico- FDA US-FDA-United State-Food & Drug Administration.MHRA-Medicines & Healthcare products Regulatory Agency-UK.TGA-Therapeutic Goods Administration-Australia. EDQM-European Directorate for Quality of Medicines-Europe.MCC-Medicinal Control Council –South Africa.ANVISA-Brazil.CE-Pharma & Medical Device.NIHS-National Institute of Health Science-Japan (Ministry of Health & Family Welfare-Japan).Solutions-• Manufacturing Problem, • Personal Problem, • Contamination Problem, • Sterilization ProblemEducational Activity-•Advance Diploma in Pharmaceutical Management (ADPM). •Master of Pharmaceutical Management (MPM).•Advance Diploma in Good Manufacturing Practice (ADGMP). •Advance Diploma in Pharmaceutical Engineering (ADPE).