GMP Fundamentals: Control of Excipients, Components and Drug Product Containers/Closures
In this course, you will learn about the fundamentals and importance of GMP control in the pharmaceutical industry. Good Manufacturing Practices (GMP), is critical for ensuring the quality, safety, and efficacy of pharmaceutical products. This includes controlling excipients, components, and drug product containers/closures to meet specific standards and requirements, reducing the risk of contamination, degradation, or incorrect formulation.
You will gain a deeper understanding of the role of GMP control in maintaining the integrity of the supply chain, and how following GMP guidelines helps ensure consumers of high-quality and safe products. By completing this course, you will have a comprehensive understanding of the crucial role GMP control plays in the pharmaceutical industry.
Included in the GMP Refresher Certificate Program
Interactive Course: What to Expect
CEUs are provided once you achieve an 80% passing grade and complete the evaluation.
The course is self-paced. On average, the time required for completion ranges from 1 to 3 hours.
Registration Fee
| Member | Nonmember |
|---|---|
| US$45 | US$50 |