Seminare zu Pharma / Medical devices
Pharma / Medical devices
High-quality courses and training for
pharma and healthcare professionals

Results FOR "Pharma / Medical devices"

SORT RESULTS

High-quality training in regulatory affairs and pharmacovigilance

Our regulatory courses and conferences are presented by established experts who will provide you with practical information on the fundamentals and trends in marketing authorisation, regulatory maintenance and post-marketing surveillance.

  • More Informations / Overview

PharmaFORUM Webcast International "Regulatory Affairs in China"

Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!

  • Online /
  • Online / 01.07. - 30.06.2019
  • Online / 01.09. - 31.08.2019
  • Online / 01.11. - 31.10.2019

Medical Writing in Pharmacovigilance

This two-day course provides an introduction to medical writing for pharmacovigilance, as well as insights into several relevant safety documents.

  • Berlin / 21. - 22.06.2018

GCP Audits in Biostatistics

This semiars informs you what to focus on to be well prepared for your next GCP audit in Biostatstics.

  • Frankfurt / 22.06.2018

PharmaFORUM Webcast International "eCTD worldwide"

Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!

  • Online /
  • Online / 01.09. - 31.08.2019
  • Online / 01.11. - 31.10.2019

Marketing Authorisation of Herbal Medicinal Products in Europe

Marketing authorisations in accordance with HMPC monographs versus purely national marketing authorisations - this course provides you with insights into national marketing authorisation requirements as well as the options in European procedures.

  • Frankfurt / 11.07.2018

Improve your Regulatory Intelligence (RI) Skills

After having attended this course, you will be aware of the key components of RI and its practical use in your role as a regulatory professional.

  • Frankfurt / 12.07.2018

Toxicology Summer School

During this course you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier.

  • Frankfurt / 08. - 09.08.2018

Variations in Europe

Variation Regulation, Classification guideline, eSubmission - all processes explained in this course.

  • Amsterdam / 27. - 28.08.2018

Medical Devices Regulatory News for 4 Continents

For all who carry responsibility in market access for medical devices in Non-EU countires with hands-on expertise, including practical examples and projects.

  • Frankfurt / Raunheim (Airport) / 30. - 31.08.2018
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