Medfiles is participating in this year’s Medicines for Europe Pharmacovigilance and Regulatory Affairs conferences in Amsterdam. Medfiles provides a wide range of regulatory and pharmacovigilance services in the Nordic and Baltic regions for companies in the pharmaceutical, medical device, IVD and veterinary sectors. Whether you need support in regulatory strategies, submissions, maintenance, translations or pharmacovigilance operations, our local experts are here to help you.
Don’t miss the opportunity to meet our professionals at the two conferences from 29 to 31 January 2020 in Amsterdam! Book a meeting with us by contacting Satu Kujala, Mikko Reiman or Tuuli Marvola directly on LinkedIn or by email. Or just drop by at out booth during the events!
[one-third-first]Satu Kujala
Scientific Advisor,
Clinical Research & Pharmacovigilance
Mob. +358 50 577 9003
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Mikko Reinman
Regulatory Affairs Manager
Mob. +358 40 187 3291
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[one-third]
Tuuli Marvola
Manager, Business Development
Regulatory affairs and pharmacovigilance services
Mob. +358 20 7441 508
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