Seminare zu Pharma / Medical Devices
Pharma / Medical Devices

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CMC Management in Regulatory Affairs

This course will give you an in-depth knowledge on the CMC requirements for the marketing authorisation.

  • Amsterdam / 25. - 26.09.2019

Pharmacovigilance EXPERT

THE course for pharmacovigilance managers!

  • Amsterdam / 29. - 30.10.2019

EU Regulatory Affairs Introductory Training Course

Do you need essential European regulatory affairs knowledge? This course gives you a compact overview about all important issues. Each day may be booked separately according to your needs!

  • Amsterdam / 25. - 27.11.2019

eSubmission Manager in Europe

The course provides practical, hands-on experience in eCTD specifications, eSubmission requirements and data integrity for IDMP, SPOR and XEVMPD.

  • Amsterdam / 18. - 19.05.2020
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