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Master of Drug Regulatory Affairs (M.D.R.A.)

Drug Regulatory Affairs

University of Bonn

Bonn, GermanyPharmaceutical Sciences
APS Requiredfull-time, part-time (study alongside work), More than 50% online

Degree

Master of Drug Regulatory Affairs (M.D.R.A.)

Language

English

Tuition

€9,900/sem

Duration

4-6 semesters

Programme Overview

This continuing-education master's programme combines pharmacy, law, and medicine in the field of drug regulation. It covers the regulatory life cycle of medicinal products and medical devices and includes twelve compulsory modules, a six-month internship, and a master's thesis.

Admission Requirements

Academic requirements

Professional experience: at least one year (relevant to the qualifying university degree)

Minimum GPA
None stated.
English requirements
English at CEFR B2.
Accepted bachelor fields
Applicants need a first professionally qualifying university degree of at least 180 ECTS in a relevant discipline such as pharmacy, biology, medicine, life sciences, or a similar field, plus at least one year of relevant professional experience at the start of the programme.
APS Certificate
Yes
Thesis required
Yes
Mandatory internship
Yes

Costs & Funding

Tuition fee
Approx. 2,475 EUR per semester based on the official total tuition of 9,900 EUR over the standard four-semester programme.
Semester contribution
115.00 EUR per semester for continuing-education students according to the official University of Bonn costs page.
ECTS credits
120
Funding info

Tuition: Approx. 2,475 EUR per semester based on the official total tuition of 9,900 EUR over the standard four-semester programme. Semester contribution: 115.00 EUR per semester for continuing-education students according to the official University of Bonn costs page.

Career Outcomes

The official programme pages list employment in the pharmaceutical industry, national and international regulatory authorities, higher federal authorities under the Federal Ministry of Health, centers for clinical studies, contract research organisations, consulting firms, law firms, ethics commissions, trade associations, and academia.

Typical job roles

Regulatory affairs specialistDrug regulatory affairs managerCompliance officerRegulatory scientistPharmaceutical industry professional

Target industries

Pharmaceutical industryMedical device industryHealth authoritiesIndustry associationsAcademia

Similar programmes in Pharmaceutical Sciences

Programme details

Degree
Master of Drug Regulatory Affairs (M.D.R.A.)
Language
English
Duration
4-6 semesters
Mode
full-time, part-time (study alongside work), More than 50% online
Start
Winter semester
Deadline
15 July (annual)

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