PharmaFORUM Webcast International
"Marketing authorisation in Turkey" 20th November 2019
- Live broadcasts every two months on current worldwide regulatory affairs and pharmacovigilance topics
- Continuing education at your workplace
- Lectures also available online at any time
- Direct communication with the experts
Aims and objectivesDo 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.
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.
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.
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.
Independent consultant on drug development, clinical trials and regulatory affairs Seda has international experience in drug development, clinical trials and regulatory affairs. Since 2010, as an independent consultant, she has been helping international companies to register and maintain their pharmaceutical products in TURKEY. Between 2004 and 2010, she worked as a consultant at PAREXEL Consulting based in the UK. Prior to that, she worked in the Regulatory Affairs Department at PFIZER Pharmaceuticals TURKEY.
Find all the details regarding the programme, experts and technical requirements at
- Six live webcasts with international experts per year
- Recorded presentations at our e-Learning Centre to review as often as you like
- Documentations for your personal download
- Multiple Choice Test after each webcast to obtain a personal certificate
This seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant local peculiarities worldwide.
13.02.2020 in Frankfurt
After completing this seminar, participants will be aware of the key regulatory requirements when preparing texts, with a greater awareness of the importance of proper English writing, reviewing and proofreading processes.
17. - 18.02.2020 in Frankfurt
Two experts will give you an in-depth update on your duties with regard to accepted clinical trial data, dossier submission and the post-approval processes.
17.03.2020 in Frankfurt