Feb 1, 2021

We are happy to announce the promotion of Katrine Schuster Ovesen from Officer to the position of Regulatory Affairs Manager.  Katrine has been with us for 6 years, starting as a student worker. She has shown an impressive ability to rapidly upskill her competences within the regulatory field, such as variation applications to all European countries and the UK as well as electronic submission requirements to the USA and Canada.

You can read more about Katrine’s qualifications here:



We are well-equipped to provide regulatory advice, discuss strategy and/or compile the registration dossier. 


We have a team of highly qualified pharmacovigilance employees with expertise in all aspects of pharmacovigilance.


We offer high quality medical & pharmaceutical translations into and from several European languages.

Electronic submission

We are equipped to assist with any type of electronic submission and maintenance of your electronic file.

Special medicines areas

Herbal medicinal products, strong vitamin and mineral products, medicinal gasses, euphoriant substances, etc.

GDP & GMP Services

We offer full time and part time responsible person (RP) function and qualified person (QP) function.