ASEAN & Chinese CTD/eCTD
Dossier content, format and submission discussed in detail
- ASEAN CTD; Chinese CTD
- CMC, efficacy and safety - data compilation
- National specialities in the various ASEAN countries
- eCTD and eSubmission
This distinguishes our event
Aims and objectivesAfter having completed these two seminar days you are aware of the regulatory novelties in China as well as of the dossier compilation challenges in China and the ASEAN countries.
On day one you will learn in detail the points to consider when applying for the marketing authorisation in China and what to keep in mind during the lifecycle of a licenced product.
Day two focusses on the dossier for marketing authorisations in China and the various ASEAN countries. After having completed day two you know the differences of the various formats and know the current status of eCTD submissions in this region.
Both seminar days can be booked separately. On day two a regulatory affairs understanding of the Chinese market is presumed (and can be obtained on day one).
It is also helpful for regulatory / medical affairs managers and business development people who aim to enter one of those markets with their products.
- ASEAN CTD versus ICH CTD
- Chinese CTD - the specifics at a glance
10:15 Coffee break
- CMC, clinical and preclinical requirements
- Dossier compilation
- Practical cases
16:00 Next step: eCTD and electronic submission
17:30 Seminar end
With over 35 years of pharmaceutical industry experience, his main area of expertise lies in pharmaceutical regulatory affairs. He was Head of Regulatory Affairs, Pharma International at Ciba-Geigy/Novartis and has been director of Pharma International regulatory consultancy for more than 10 years.
She has several years‘ experience in regulatory affairs in the Asia-Pacific region, most recently as DRA Manager FE Countries at a Swiss pharmaceutical company.
Phone: 069 2561790
May we also draw your attention to our seminar
"Regulatory Affairs China"
on the 17 March 2020 in the same conference hotel.
You will find detailed information on www.forum-institut.de with web code 2003231.
By attending both courses, you will benefit from a € 190 (+VAT) discount
Good overview / AP-Registrations
I got a completet overview and I am looking forward to getting the following course eg practical use e-CTD
Nice atmosphere and professional information
Viel praktisches Wissen
To have a good overview for nearly all Asean countries and China with MAA and clinical trials
Very good seminar
Low participants number - you can alsways ask questions
Good overview, get individual questions answered
Speakers with a lot of experience
CHEPLAPHARM Arzneimittel GmbH
Information regarding country specific
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!
01.11. - 31.10.2020 in Online
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.
31.12.2019 in Online
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