PharmaFORUM Webcast International "Clinical trials in China" - 26 September 2019

- Chinese regulatory authorities overview
- CTA procedures including CTA filing and approval
- CTA relevant requirements, such as CTA dossier preparation, foreign clinical trial data acceptability, interaction with authorities

Do you work in international regulatory affairs or pharmacovigilance? We would like to invite you to join our live webcasts, where local regulatory affairs and vigilance experts will inform you every two months of the latest news and trends in global marketing authorisation and drug safety.
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You will meet our experts in a virtual conference room and share your experiences in regulatory affairs and pharmacovigilance within and beyond the ICH region.
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Each meeting will be held as a 1.5-2-hour webcast, presenting the latest news with supporting presentation slides. To be best prepared, you will be able to download the complete presentation documents prior to each webcast.
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Are you unable to attend one of the webcasts? No problem! Following each live meeting, you will be able to retrieve the recorded webcast (audio track 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.

Termin

Datum: 01.09.2019
Ort: Online

- Online
Preis: 900,00 EUR zzgl. MwSt.
 

Zielgruppe

This webcast series addresses the needs of managers in the pharmaceutical industry, who need to keep up to date in global regulatory affairs and pharmacovigilance.

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