The Key Points of Compliance System Construction for Sterile Drug Manufacturers
Автор: AUSTAR TECHNICAL SERVICE
Загружено: 2026-01-30
Просмотров: 0
Описание:
Discover how to build a robust, audit-proof compliance system for sterile drug manufacturing with Andrew Marshall, a veteran with 30 years of experience at Novartis, GSK, Merck and the UK NHS.
This masterclass covers the core principles of Pharmaceutical Quality System (PQS), critical audit focus points, non-negotiable sterile production requirements, and proactive monitoring strategies adopted by leading global pharmaceutical enterprises. Turn regulatory compliance from a risk point into a core competitive advantage, and build a compliance system that can pass rigorous official and client audits.
#SterileDrugs #PharmaceuticalCompliance #PQS #DrugManufacturing #RegulatoryAffairs #GMP #AuditPreparation #PharmaceuticalIndustry #QualityManagement
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