Workshop Training / course
How to Navigate the Parallel HTA and EMA Processes in the EU
Drug Information Association (DIA)
- When One day, 11:00 Europe/Zurich Add to calendar
- Where Basel, Switzerland Venue Congress Center Basel, Messeplatz 21, Basel Show on map
- Format In person Online
- Admission Paid Register
- Topic Regulatory
Key dates
- DIA industry member early RATE cutoff Registration Closes in 99 days Register
- The event begins One day In 155 days
About this event
A one-day, in-person DIA training course in Basel on running EU Joint Clinical Assessment alongside EMA marketing authorisation, now required for cancer medicines and advanced therapies. It explains how the two processes link, what information regulators and HTA bodies share, and how to plan evidence, align teams and manage dossier submission. Faculty have worked closely on implementing the HTA Regulation, and small-group workshops make it practical. It suits regulatory strategy, market access and clinical development professionals, CROs and consultants.
Who it is for
- Regulatory affairs
- HTA
- Market access
- Clinical development
Organiser
Checked 11 Oct 2026 Checked against the organiser's page on 11 October 2026. Dates and prices can change: confirm with the organiser before you book.
Location
Congress Center Basel, Messeplatz 21, Basel, Basel, Switzerland