Fda Pharmaceutical Industry Drug Development Quality Assurance Biotechnology Pharmaceutics Regulatory Submissions Biopharmaceuticals Capa Quality Auditing Gmp Sop Quality System Change Control Lifesciences Clinical Trials Aseptic Processing Manufacturing Quality Management Regulatory Requirements Ind Technology Transfer Regulatory Affairs 21 Cfr Part 11 Iso 13485 Medical Devices Validation Computer System Validation Gxp Iso Glp Lims V&V Gcp Cleaning Validation Analytical Chemistry Clinical Development Cro R&D Pharmacovigilance Gamp Design Control Quality Control Regulations Iso 9000 Protocol Vaccines Formulation Ctms Life Sciences
Interests:
Electronics
Certifications:
Rac Qms Lead Auditor Designated Representative License, Drug Wholesaler Dea License Raps Irca Rab Qsa Board of Pharmacy, California Dea