Executive Development Programme in GMP and Regulatory Change
-- ViewingNowThe Executive Development Programme in GMP & Regulatory Change is a certificate course designed to provide professionals with the latest insights and skills in Good Manufacturing Practices (GMP) and regulatory compliance. This program is crucial in today's pharmaceutical and healthcare industries, where staying updated with regulatory changes is essential for business success and compliance.
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โข Introduction to GMP (Good Manufacturing Practices): An overview of GMP, its importance, and key principles.
โข GMP Regulations and Guidelines: A deep dive into global GMP regulations and guidelines, including ICH Q7, EU GMP, and FDA GMP.
โข Quality Management System (QMS): Understanding the role of QMS in GMP, including ISO 9001 and its relationship to GMP.
โข GMP for APIs (Active Pharmaceutical Ingredients): An examination of GMP requirements for APIs, including ICH Q7 and cGMP.
โข GMP for Sterile Products: A study of the unique GMP requirements for sterile products, including aseptic processing and sterilization.
โข GMP for Biologics: An exploration of the specific GMP requirements for biologics, including cell banking, viral clearance, and product characterization.
โข Regulatory Change Management in GMP: Best practices for managing regulatory change, including impact assessments, risk management, and communication strategies.
โข GMP Audits and Inspections: Preparing for and managing GMP audits and inspections, including FDA, EMA, and other global regulatory authorities.
โข GMP Trends and Future Developments: An examination of current trends and future developments in GMP, including continuous manufacturing, real-time release, and data integrity.
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