Single Course Pharma & Cosmetics

Introduction to 21 CFR 210/211 GMPs For Finished Pharmaceuticals Training

Through interactive training, for participants to learn to interpret and apply the FDA requirements for production, quality systems, and management of finished pharmaceuticals: 21 CFR 210 and 211.

1-Day Virtual Class English Identifier: 193676467
Introduction to 21 CFR 210/211 GMPs For Finished Pharmaceuticals Training

Course Overview

What you'll learn

Upon completion of this course, learners will be able to:

  • Explain and define GMP and cGMP.

  • Discuss the role of the FDA in the cGMP process.

  • Describe the types of inspections and potential outcomes for cGMP.

  • Understand and apply the information to your everyday roles and responsibilities

Who This Course Is For

  • Manufacturers, test laboratories, packagers (including pharmacies).

  • Directors, managers, supervisors.

  • Engineers, Auditors, Manufacturing personnel, Quality control and Assurance personnel.

  • Corporate personnel supporting cGMP activities and Laboratory personnel.

About this course

This 1-Day course is designed through interactive training, for participants to learn to interpret and apply the FDA requirements for production, quality systems, and management of finished pharmaceuticals: 21 CFR 210 and 211. Learners will discuss ways to minimize or eliminate issues related to contamination, mix-ups, superpotency/sub-potency, misbranding, bioavailability, and safety and efficacy.

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