Good Manufacturing Practice (GMP) in relation to GCP – eLearning

Reasons to attend

You want to know where investigational products come from, how they are made and what rules and regulations have to be followed?

You are working with Investigational Medicinal Product (IMP), you already have the knowledge of Good Clinical Practices and now you need to be able to link it to the good manufacturing practices?

Then register for this eLearning course. We cover from raw material until IMP destruction to help you manage IMP properly within your Clinical Trial. Good Manufacturing Practice, Good Clinical Practice and Good Distribution Practice will hold no secrets anymore.

What's included?

• Documents and materials related to this course are included
• Globally recognised certificates awarded after test completion
• This course has been reviewed by the Belgian GCP Inspectorate.

Course schedule

• Course credit: 6h (3 months period to complete course)
• Complete the course at anytime, anywhere!

Course Description

This GMP and GCP training is designed for professionals who are involved in the handling of investigational medicinal products. Through an interactive approach this eLearning course targets monitors, project managers, site personnel, or administrative persons who are responsible for sending, storing, accountability, final disposition, etc. of medicinal products used in clinical trials. In addition, professionals who are in charge of or supervise packaging, randomisation and allocation or labelling of investigational medicinal products will benefit from this course.

Optionally you can also get an overview of the latest regulatory standards set by the European Union including Directive 2001/20/EC, 2003/94/EC, 2005/28/EC, Annex 13 of EC-GMP Guideline, ICH GMP Q7, ICH GCP E6; 2013/C343/01 (GDP)and 2013/C 68/01 guidelines.

Interactive quizzes and exercises for self-assessment are included to provide a better understanding of each part of the course. You will be able test your comprehension with a final grading assessment.