Pharmaceutical Regulatory Affairs and IPR

Muhammad Naeem has 19 plus years diversified experience in Quality Operations, Regulatory Affairs, Research and development and Operational Excellence. He is RAC-Global certified. He is an active member of ISPE, PDA and RAPS, USA. He has an extensive knowledge of ICH, USP, BP, and HACCP. He has lead 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. He has attended many national and international conferences as a speaker on Quality Risk Management, Data integrity, Pharmacovigilance, QMS elements, Validation,

cGMP Guidelines, etc.