Ensure every autoclave, reactor, and clean-room asset is specified, installed, and proven fit-for-use by mastering the full GMP equipment-qualification lifecycle—planning, IQ/OQ/PQ execution, and performance monitoring—in line with EU GMP Annex 15, giving you audit-ready expertise as an Equipment Qualification Specialist.
Developed by Zamann Pharma Support, a TÜV ISO 9001-certified quality management service provider for European pharmaceutical companies,