View, browse and sort the ever-growing list of sessions by pass type, track, and format. With this Session Scheduler, you can build your schedule in advance and access it during the show via export or with the Mobile App, once live. Sessions do fill up and seating is first come, first serve, so arrive early to sessions that you would like to attend.
Muhammad Naeem has 20 plus years diversified experience in Quality Operations, Regulatory Affairs, Research & Development and Operational Excellence. He is RAC-Global certified from RAPS as well as an active member of RAPS-USA, ISPE & PDA. He has an extensive working knowledge of FDA, EMEA, WHO, ICH, USP, BP, and other global regulations for Pharmaceuticals.
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 multiple topics like Quality Risk Management, Data integrity, Pharmacovigilance, QMS elements, Validation, cGMP Guidelines, etc. Currently, he is serving as Chief Operating Officer (Technical) at Indus Pharma.