M.Sc. in Regulatory Writing

Msc in Regulatory Writing

Today, we are proud and excited to announce a new cooperation as part of our Corporate Responsibility Program.

Evnia has joined forces with Università degli Studi di Siena, one of the oldest European Universities to create a unique Masters’ Program in Regulatory Writing!

In a time when the regulatory framework in Europe is rapidly changing (see implementation of MDR, IVDR, new Clinical Trials Regulation), this new, one-year-long, smartly designed “M.Sc. in Regulatory Writing” aims to train the future regulatory writers with the help of well-established, professional regulatory specialists, who will be delivering theoretical-practical lectures!

Here are some of the program’s Modules will include:

  • Regulatory strategy for medical devices
  • Clinical Evaluation Plans and Clinical Evaluation Reports
  • Market authorization for medicines
  • eCTD
  • Development strategy for COVID-19 vaccines
  • Orphan Drugs
  • Medicines for pediatric populations

Through this partnership, Evnia will cover both running costs and 2 scholarships during the first year, after which our contribution will be further increased!

Supporting continuous training and #Education is in the core of Evnia’s Ethos.
We Strive for Knowledge, We Seek new Partners, We Find Solutions!

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