Master the origins, concepts, guidelines, and industry standards of Good Manufacturing Practices (GMPs). This certification offers a comprehensive overview of the current EU GMP Part I requirements applicable to the manufacture of medicinal products in the European Union.

Chapter/Module/Course title: 

Course 1: The origins of GMP in the GxP Industry

Description: Explore the origins of GMP regulations in the pharmaceutical industry, from historical tragedies to modern regulations. This three-part course begins with the foundational concepts.

Course 2: Fundamentals of Good Manufacturing Practices

Description: Learn key concepts, primary guidelines, and the fundamentals of Good Manufacturing Practices (GMP) for ensuring quality in pharmaceutical manufacturing.

Course 3: Good Manufacturing Practices for Medicinal Products (EU GMP Part I)

Description: Master the principles and guidelines of GMP for medicinal products for both human and veterinary use, as outlined in EU directives.

Additional Information

• Who should attend: This certification is recommended for professionals involved in pharmaceutical manufacturing, quality assurance (QA), regulatory affairs, and those seeking a comprehensive understanding of GMP.

• Certification Duration: Approximately xxx hours

• Skill level: Beginner-Intermediate

• Final assessment: Yes (x quizzes)

• Certification associated: Yes