eLearning Part 1: Introduction to GMP and Quality Systems

Short description

GMP Part 1 covers the following topics:

• Introduction to GMP
• Quality Systems
• Deviations and Out of Specifications (OOS)
• Pharmaceutical Documentation
• Change Control

The total course will take about 170 minutes to complete, but you can do it at your own pace and in your own time. The course is in English.

Procedure:

After your registration you will receive an invoice from us.

Upon receipt of your payment, we will send you a link to the course.

Once you have notified us that you have completed the course, you will receive a certificate.

Objectives

• Understanding the meaning of GMP and becoming familiar with commonly used terms
• Realizing the importance of working under GMP
• Gaining insight on the pharmaceutical chain and the life-cycle of (bio)pharmaceutical products
• Understanding the main quality systems procedures such as change control, deviations, corrective en preventive actions (CAPAs), and Out of Specifications
• Getting familiar with documentation types and document management in a GMP environment

Target group

Who Should follow this GMP Course?

(New) employees within a (bio)pharmaceutical production or analytical environment with limited GMP experience who would like to learn the basics on GMP

Experienced GMP professionals who would like to refresh their GMP knowledge (e.g. for annual GMP training).