Requirements

Requirements

In order to maintain a professional level in the programme, applicants are required to have, as a minimum, a
relevant Bachelor Degree and 2 years of experience within Regulatory Affairs from the pharmaceutical/biotech industry or regulatory authorities, or similar qualifications.

Applicants, who do not meet the entry requirements, will be considered on a case-by-case basis. Lack of formal qualifications need not be a barrier to study, and exemptions may be granted case by case. For each module, Medicademy will accept for up to 20 % of the seats to be occupied by applicants with limited experience within the Regulatory Affairs area, as long as they are able to benefit from and actively participate in the module activities.

Approximately 25 applicants will be admitted to each module. Please note that applications will be considered in order of receipt.

	Regulatory Affairs
	Pharmacovigilance
	Individual Courses
	E-learning

SEE THE COURSE CALENDAR HERE

Stine Folkenberg Hedegaard

Stine Folkenberg Hedegaard is E-learning Manager and responsible for e-learning, communication, marketing and a number of courses.

sfh@dli.dk

Phone: +45 39 15 09 27

Helle Rishøj Nielsen

Helle Rishøj Nielsen is Payroll Officer and is responsible for payroll, travel arrangements, evaluations, diplomas and certificates, etc.

hrn@dli.dk

Phone: +45 39 15 09 11

Minna K. Jørgensen

Minna Kjær Jørgensen is Program Director, Medicademy Pharmacovigilance and also responsible for Introduction to Safety & Pharmacovigilance and Medical Advertising Standards.

mkj@dli.dk

Phone: +45 39 15 09 28

Tina Jensen

Tina Jensen is Program Director, Medicademy Regulatory Affairs and responsible for Introduction to Drug Registration.

tj@medicademy.net

Phone: +45 39 15 09 14

Henrik Køhler Simonsen

Henrik Køhler Simonsen is Head of Department and Head of Lif Education, Lif Exhibition and Medicademy.

hks@dli.dk

Phone: +45 39 15 09 45