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2005958 Webcast Clinical Trials
PharmaFORUM Webcast Clinical Trials "Investigational Medicinal Product: EU GMP Annex 13 Versus Regulation EU No 536/2014"
2020-06-04 2020-06-04 online

PharmaFORUM Webcast Clinical Trials "Investigational Medicinal Product: EU GMP Annex 13 Versus Regulation EU No 536/2014"

7 May 2020

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.
Topics
  • Present and future challenges for clinical investigational products, such as labelling requirements
  • IMP supply chain management

Aims and objectives

Do you work in clinical trials? Then we would like to invite you to our live webcast in which experts from clinical research will inform you about the latest updates and trends in clinical studies within and beyond the ICH region. You will receive information on the design and conduct of clinical trials, as well as practical tips for successful collaboration at the interfaces to other areas. You will meet our experts in a virtual conference room. Each meeting will be held as a 1.5 - 2 hour live webcast, presenting the latest news with supporting presentation slides (also for your personal download). Your practical questions will be addressed directly via the chat function, coordinated by the meeting's chairperson. Are you unable to attend one of the webcasts? No problem! After each live meeting, you will be able to retrieve the recorded webcast (audio and presentation) from our eLearning Centre, using your personal password. This allows you to review each presentation at any time and as often as you like. An optional multiple-choice test finalises each webcast, giving you the possibility to receive a personal certificate.
Who should attend
This webcast series addresses the needs of managers in the pharmaceutical industry, who need to keep up to date with the design and management of clinical trials.
Referenten
Ihre Referenten
Dr. Claudio Lorck
Keine kurze englische Beschreibung vorhanden


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