Seminare zu Online-Training
Online-Training
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Global Regulatory Affairs Manager

This online training addresses the needs of regulatory affairs managers dealing with marketing authorisations outside the EU or planning to do so in the future.

  • Modular e-Learning and webcast / Access possible at any time

Development Expert Biologics

  • Modular e-Learning and webcast / Access possible at any time

eCTD preparation and submission

This online training programme consisting of three recorded webcasts will train you how to develop documents, compile them and submit an eCTD step by step.

  • Online /
  • Online / 31.12.2020

e-Learning: Introduction to EU Marketing Authorisation

This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe (MRP, DCP, CP) . It will also introduce you to post-authorisation duties (renewal, variation...).

  • Online /

e-Learning: Marketing Authorisation Outside the ICH Region

This e-learning will familiarise you with the regulatory affairs principles outside the ICH region and show you how to categorise the various regions in terms of regulatory requirements. Dossier requirements in Australia, Hong Kong, India, South Korea, Taiwan, Saudi Arabia, GCC, Jordan, Turkey, Thailand, China, South Africa, Russia, Kazakhstan, Eqypt, Brazil, Mexico & Argentina will be addressed

  • Online /

e-Learning: Common Technical Document & eCTD

Do you need know how regarding CTD/eCTD & CMC? Then this e-learning programme is the fast track to becoming knowledgeable in this field. No prior dossier experience is required.

  • Online /

e-Learning: Stability Testing in the ICH Region

This e-Learning programme will focus on stability testing for chemical and biological pharmaceutical products in the ICH region.

  • Online /

e-Learning: CTD Module 3

This e-Learning programme will familiarise you with the data requirements in CTD Module 3.

  • Online /
  • Online / 31.12.2020

First Accredited Diploma in Pharmacovigilance for the Middle East

First Accredited Diploma in Pharmacovigilance for the Middle East

  • Online /

PharmaFORUM Webcast International

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 /

PharmaFORUM Webcast Clinical Trials

Our experts will update you every month with the latest updates and trends in clinical studies. Thus, you will always have essential information on the design and conduct of clinical trials, as well as practical tips for successful collaboration at the interfaces to other areas.

  • Online /

eCTD preparation and submission

This online training programme consisting of three recorded webcasts will train you how to develop documents, compile them and submit an eCTD step by step.

  • Online /
  • Online / 31.12.2019

Webcast Series: Legal Issues in Regulatory Affairs

These recorded six webcasts enable you to deal with the legal challenges in marketing authorisation and life cycle management.

  • Online /

Pharmacovigilance in Europe - Introductory e-Learning

Do you need to be well versed in European pharmacovigilance for your daily work? Then we recommend this e-Learning. You can choose between three different packages according to your level of expertise and requirements.

  • Online /

e-Learning: Stability Testing in the ICH Region

This e-Learning programme will focus on stability testing for chemical and biological products in the ICH region.

  • Online /

e-Learning: CTD Module 3

This e-Learning programme will familiarise you with the data requirements in CTD Module 3.

  • Online /
  • Online / 31.12.2019
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