Helis Academy GMP course for academics and professionals (level II) Belgium

Always wanted to work in the pharmaceutical industry, but lacked the necessary experience? With this ten-day course you will not only increase your knowledge, but also your practical experience.

Academy 10-day course for academics and professionals on ‘Good Manufacturing Practices’ in (bio)pharmaceutical production (level II), June 7-18, 2021

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.

>>>   CLICK HERE FOR MORE INFORMATION & THE PROGRAMME   <<<
REGISTER NOW!

Target group

The Level II 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).

Practical information

What?

The course consists of two parts, a part on quality management systems and a part on processing. We strongly recommend to register for the complete 10-day course, because it will touch all important aspects of GMP and prepare you well for the pharmaceutical industry. However, it is also possible to register for the two parts separately.

When? From 7-11 June 2021: module 1-5. From 14-18 June 2021: module 6-10.

Where? Quality by Design NV, Fotografielaan 5, 2610 Wilrijk, Belgium. Except for module 6 and 7 (14-15 June), which will take place at Advipro, Wechelsebaan 143 Unit 13, 2275 Lille, Belgium.

Registration fee?

  • Full course
    The registration fee for the ten-day course is €2745 (excl. VAT) for flanders.bio members and €2995 (excl. VAT) for non-members. The registration fee for students and job seekers (private rate) is €495 (excl. VAT).
  • Part I
    The registration fee for the five-day course is €1375 (excl. VAT) for flanders.bio members and €1500 (excl. VAT) for non-members. The registration fee for students and job seekers (private rate) is €250 (excl. VAT).
  • Part II
    The registration fee for the five-day course is €1370 (excl. VAT) for flanders.bio members and €1495 (excl. VAT) for non-members. The registration fee for students and job seekers (private rate) is €245 (excl. VAT).
CLICK HERE FOR MORE INFORMATION & THE PROGRAMME
REGISTER NOW!