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Regulatory Science● OpenMastersPreview

Master of Drug Regulatory Affairs (MDRA)

An interdisciplinary postgraduate programme combining pharmacy, law, and medicine to prepare professionals for careers in drug regulatory affairs.

Best for:Working professionals in pharmacy, medicine, or life sciences seeking to specialize in regulatory affairs and pharmaceutical compliance.

University of Bonn · Bonn, Germany · R1 · First-stage researcher
More professors at University of Bonn
Regulatory AffairsPharmaceutical LawDrug SafetyMarket AccessMedical DevicesQuality Management
This is a masters position — not a PhD studentship.
Deadline
Register by 16 March 2027
Funding
—
Tuition fee (one-off): 9,900 EUR
Start date
Winter semester
Location
Bonn
Germany

Overview

The Master of Drug Regulatory Affairs (MDRA) at the University of Bonn is an interdisciplinary programme designed for professionals seeking specialized training in the regulation of medicinal products and medical devices. Developed in cooperation with the German Society for Regulatory Affairs (DGRA), the curriculum covers essential topics such as quality, safety, efficacy, market access, and document management. The programme is delivered through a flexible format that is over 50% online, allowing students to balance their studies with professional commitments. Participants benefit from a network of senior experts from health authorities and the pharmaceutical industry, gaining practical insights into the regulatory landscape.

Regulatory AffairsPharmacyPharmacovigilanceDrug DevelopmentHealthcare PolicyLife Cycle Management

What you'll do

  • Complete 12 modules covering regulatory science, healthcare policy, and pharmaceutical law.
  • Participate in both online lectures and on-site sessions in Bonn.
  • Execute written study papers and project work for module assessments.
  • Undertake a compulsory internship to apply regulatory knowledge in a professional setting.
  • Conduct independent research and write a Master's thesis on a relevant regulatory topic.

Requirements

Degree required: University degree in pharmacy, biology, medicine, life science, or a related field.

Degree offered: Master of Drug Regulatory Affairs (MDRA)

Language: English; B2 level (e.g., IELTS Academic 6.0, Cambridge B2 First).

Instruction: English

Required skills
  • At least one year of professional experience relevant to the qualifying university degree.
  • English language proficiency at B2 level or higher.
  • Ability to engage in interdisciplinary study across pharmacy, law, and medicine.
Nice to have
Prior experience in the pharmaceutical or healthcare industry.Familiarity with clinical trial processes or medical device regulations.
Eligibility
  • Must hold a professionally qualifying university degree in a relevant scientific or medical field.
  • Must have at least one year of relevant professional experience.

Funding & terms

Type
Unknown
Amount
Tuition fee (one-off): 9,900 EUR
Duration
4 semesters (full-time) or 6 semesters (part-time)
Programme
—

Programme and admissions

Admissions not verified

A catalogue listing does not mean applications are open or funding is guaranteed. Check the source for your intake.

Intake
Not confirmed by the source
Duration
Not confirmed by the source
Teaching language
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Taught / research mode
Not confirmed by the source
Study mode
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Campus
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Prerequisites
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Application instructions
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Tuition
Not confirmed by the source
Funding
Not confirmed by the source

How to apply

Deadline: 2027-03-16

Applications must be submitted to the Examination Board of the Master's degree programme for continuing education at the University of Bonn. Detailed instructions and required documentation can be found on the official DGRA application website.

Documents required
  • Academic transcripts
  • Proof of professional experience
  • English language certificate
↗Check programme and admissions

Contact

Jasmin Fahnenstich· Examination Board

https://www.dgra.de

Lab
DGRA e.V. – Deutsche Gesellschaft für Regulatory Affairs
University of Bonn
Germany
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