The Good Manufacturing Practices (GMP) for Pharmaceutical and Medical Devices Professional Diploma offers specialized training in the stringent quality standards and regulatory requirements specific to the pharmaceutical and medical devices industries. This program covers critical areas such as facility design, equipment validation, documentation practices, quality assurance, and regulatory compliance. Participants will gain the expertise needed to ensure the safety, efficacy, and quality of pharmaceutical products and medical devices throughout the manufacturing process. Graduates will be equipped to implement and maintain GMP protocols, adhere to regulatory guidelines, and uphold the highest standards of product quality and patient safety in these highly regulated sectors.

Module Titles

• Medical Devices Directive & Regulations & Reporting
• Medical Devices Risk Management
• Medical Devices Post Market Surveillance and Vigilance
• Implementing & Managing Quality Management System in Medical Devices
• Clinical Evaluation of Medical Devices
• Management and Behavioral Skills in Quality Assurance

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