Always wanted to work in the pharmaceutical industry, but lacked the necessary experience? Flanders.bio is organizing ten-day course where you will not only increase your knowledge, but also your practical experience.
The production of medicines is a profession with its own challenges. Medicines must meet high standards before they can be administered to patients. This means, among other things, that medicines are manufactured in a very clean environment where strict quality controls are in place. The guidelines for the production of medicines have been laid down by the EU as Good Manufacturing Practice (GMP).
This course covers the essential aspects of (bio)pharmaceutical manufacturing. Through lectures, practical lessons, workshops and guided tours, you will get a complete picture of, and good insight into all things related to GMP. Advipro has a complete training center with a cleanroom, which means that you can immediately apply the acquired knowledge in a realistic practical environment.
Whether you are interested in a job that involves the development of analytical methods, production, quality control, quality assurance or process development, this course provides a good basis for a job in the biotech or pharmaceutical industry.
Through lectures, practical lessons, workshops and guided tours you will get a complete picture of and a good insight into the topics below:
This GMP course is aimed at graduates (BSc, MSc, PhD and postdoc)and professionals, who have studied a subject or discipline in Life Sciences, but have no experience in the GMP production industry. If you want to know more about the (bio)pharmaceutical production industry then this course is something for you. With this course you will gain insight and experience in the pharmaceutical manufacturing industry. You could then qualify for jobs in production, quality control (QC), analytical method development, formulation development or quality assurance (QA).
Module 1: Introduction to Good Manufacturing practices (GMP)
Module 2: Quality management system and documentation
Module 3: Contamination control: infrastructure - staff – cleaning – Organised by Advipro
Module 4: Aseptic techniques – Organised by Advipro
Module 5: Quality Management System: deviations - OOS - change control
Module 6: Raw materials, packaging/labelling and distribution
Module 7: Validation (Facility/equipment/system qualification and Process validation)
Module 8: Quality Control
Module 9: Downstream processes
Module 10: Aseptic production filling
For more detailed information you can visit the website of Flanders.bio.