Pharmaceutical Regulatory Affairs and IPR

Muhammad Naeem has more than 19 years diversified experience in quality operations, regulatory affairs, research and development. He has done certificate courses on cGMP, GLP, Process Validation, ISO/IEC 17025:2005, 14001:2004, OHSAS 18001:2007, SA 8000 and 9001:2008. He is a Member of International Society for Pharmaceutical Engineering (ISPE) and Regulatory Affairs Professional Society (RAPS), USA. He has extensive knowledge of ICH, USP, BP, ASTM, and HACCP and has led several investigational/developmental and technical/analytical projects at CMOs in USA, Europe and Pakistan. Some of the major pharmaceuticals he served are Pfizer & Takeda (USA), CCL Pharmaceuticals and INDUS Pharma, Pakistan. He has strong scientific, analytical, planning, managerial and training skills.