GMP Pharma 210-211 Requirements

This ON DEMAND 8-hour e-course teaches a detailed understanding of the concepts and requirements of FDA 21 CFR 210 and 211 Pharmaceutical CGMP regulations. Includes a certified training Certificate of Competence. 0.8 CEUs.

Buy $300.00

Course curriculum

1. How to use this course
1. FDA-GMP-Pharmaceutical_Lesson-02
2. FDA-GMP-Pharmaceutical_Lesson-02_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-03
2. FDA-GMP-Pharmaceutical_Lesson-03_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-04
2. FDA-GMP-Pharmaceutical_Lesson-04_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-05
2. FDA-GMP-Pharmaceutical_Lesson-05_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-06
2. FDA-GMP-Pharmaceutical_Lesson-06_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-07
2. FDA-GMP-Pharmaceutical_Lesson-07_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-08
2. FDA-GMP-Pharmaceutical_Lesson-08_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-09
2. FDA-GMP-Pharmaceutical_Lesson-09_QUIZ
1. FDA-GMP-Pharmaceutical_Lesson-10
2. FDA-GMP-Pharmaceutical_Lesson-10_QUIZ
1. Congratulations

About this course

$300.00
20 lessons
0 hours of video content

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Velocity 360 USA Training | UK

GMP Pharma 210-211 Requirements

Course curriculum

Welcome to the course!

Introduction - GMP Pharma

Terms and definitions

Subpart A – General Provisions | Subpart B – Organization and Personnel | Subpart C – Buildings and Facilities

Subpart D – Equipment

Subpart E – Control of Components and Drug Product Containers and Closures

Subpart F – Production and Process Controls

Subpart G – Packaging and Labeling Control

Subpart H – Holding and Distribution | Subpart I – Laboratory Controls

Subpart J – Records and Reports | Subpart K – Returned and Salvaged Drug Products

Next Steps

About this course

Discover your potential, starting today