International Development and Registration of Medicine and Health Products 12 months Postgraduate Programme By Université Paris-Saclay |TopUniversities

International Development and Registration of Medicine and Health Products

Programme Duration

12 monthsProgramme duration

Tuitionfee

243 EURTuition Fee/year

Main Subject Area

Medicine Related StudiesMain Subject Area

Programme overview

Main Subject

Medicine Related Studies

Degree

MSc

Study Level

Masters

Study Mode

On Campus

The objectives of this program are to train drug professionals by deep diving into the scientific and regulatory aspects of pre- and post- marketing authorisation drug development and registration, at a strategic and operational levels, with an international focus: European Union, USA, Canada, Switzerland, Australia, Japan, South-East Asia (China, Korea, India...), ASEAN region, Russia and EEU region, Central and Eastern region, Middle-East region, Africa, Latin America (Argentina, Brazil, Mexico...)...
This program leads to positions in Regulatory Affairs in pharmaceutical companies (headquarter or affiliates), pharmaceutical regulatory affairs consulting services or national and international agencies of health products for humans or animals, in numerous countries around the world, with the following missions: regulatory strategy of drug development and registration, drug product post-approval activities, pharmacovigilance and risk management, regulatory compliance, regulatory intelligence...
In order to apply to one of the programmes of the master, please select the programme you are interested in under the "Year 1 & 2 Master's programmes" tab .

Programme overview

Main Subject

Medicine Related Studies

Degree

MSc

Study Level

Masters

Study Mode

On Campus

The objectives of this program are to train drug professionals by deep diving into the scientific and regulatory aspects of pre- and post- marketing authorisation drug development and registration, at a strategic and operational levels, with an international focus: European Union, USA, Canada, Switzerland, Australia, Japan, South-East Asia (China, Korea, India...), ASEAN region, Russia and EEU region, Central and Eastern region, Middle-East region, Africa, Latin America (Argentina, Brazil, Mexico...)...
This program leads to positions in Regulatory Affairs in pharmaceutical companies (headquarter or affiliates), pharmaceutical regulatory affairs consulting services or national and international agencies of health products for humans or animals, in numerous countries around the world, with the following missions: regulatory strategy of drug development and registration, drug product post-approval activities, pharmacovigilance and risk management, regulatory compliance, regulatory intelligence...
In order to apply to one of the programmes of the master, please select the programme you are interested in under the "Year 1 & 2 Master's programmes" tab .

Admission Requirements

72+
5.5+
Compulsory supporting documents
  • Certificate of English level.
  • Curriculum Vitae.
  • All transcripts of the years / semesters validated since the high school diploma at the date of application.
  • Motivation letter.
Additional supporting documents
  • Detailed description and hourly volume of courses taken since the beginning of the university program.
  • Choice sheet of M2 (obligatory for the candidates registered in M1 at the University Paris-Saclay) to download on universite-paris-saclay.fr
  • Certificate of French (compulsory for non-French speakers). (Level B2 required)
  • VAP file (obligatory for all persons requesting a valuation of the assets to enter the diploma).

1 Year
Jan
Sep

  • Candidates are required to submit references or letter(s) of recommendation for acceptance
  • Candidates are required to submit an essay(s) for acceptance

Domestic
243 EUR
International
243 EUR

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