Medhouse Academy

Our Courses

Regulatory Affairs Advanced

Date: June 12 (1 day)
Price: 6900 SEK per participant
Place: Digitally
Course language: English
Diploma: Certificate is awarded after completion of the course


This advanced course is a comprehensive extension of the RA essentials course and is relevant for those who need further insights in Pharmaceutical Development. This course will show how RA applies from early drug discovery and preclinical trials – to – market authorization (MA) applications, approvals (launch) and  optimizing the important life cycle management. 

From a regulatory affairs perspective the course will not only indicate strategic preparations before launch but also key strategies during lunch and after patent has expired. The aim of the course is to give the delegates professional reputation building, career and product success enhancement through proper understanding of advanced Regulatory Affairs and related concepts. The delegates will have a test after the course and then receive a certificate in Advanced Regulatory Affairs.

The lecturer for the RA Advanced course is Ingela Frick. She is a strategic and business driven senior leader with experience from big global- as well as small Swedish companies. She is used to leading companies through changes, acquisitions and mergers and has strengths within regulatory, quality and pharmacovigilance, and late phase development together with launch preparations of pharmaceuticals.

Let us know if you have any questions


Other exciting courses