Priyank Srivastava, R.Ph

New Delhi Area, India India

Regulatory Affairs Specialist: Medical Devices, IVD's, Drugs, API's, Biologicals

Medical / Health Care / Pharmaceuticals

Having work experience of around Six years in various spheres of Pharmaceutical Profession. Before joining Regulatory Affairs, had opportunity to work as QA & QC Head. This prior experience has helped me to visualize the problem and has proved boon to a great extent in getting solutions, which is the prime requirement for any Regulatory Specialist.  Central Drug Standard Control Organization New Delhi (CDSCO). Medical Devices (extensively with Class II and Class III devices viz. Cardiac Implants, Orthopedic Implants, Grafts, Dental Implants and almost all Notified Devices and for that applying and received more than hundred registrations), Diagnostics Kits (Critical, Semi-critical and .