Conference · Basel, Switzerland
Essentials and Overview of the Regulatory Framework in Europe
Health
Key numbers
- Editions on record
- 1first in 2016
About Essentials and Overview of the Regulatory Framework in Europe
The course will give an overview of the European regulatory system for human medicines, including the legislative processes and European networks, the different routes for obtaining a licence for the European market, the centralised, the decentralised and the mutual recognition procedures, and the national procedures. Different steps and timelines for the various procedures will be covered. An introduction to pharmacovigilance, variations and renewals will be given in the context of the lifecycle. In addition, the specific European procedures for orphan drugs, paediatrics, advanced therapies and combination products will be discussed. The course will cover the current registration systems available for approval of human medicinal products: - Regulation EC726/2004 on the centralised procedure, including specific marketing authorisations and the European Medicines Agency - Directive 2001/83/EC 'the Community Code' on the Mutual Recognition Procedures A case study will enable participants to apply the freshly gained knowledge into their daily practice. This is a hands-on course. It is necessary that you bring your laptop/electronic device with you.
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2016 | 21–22 Nov 2016 | Dorint An Der Messe Basel Basel, Switzerland | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.
Questions
When is Essentials and Overview of the Regulatory Framework in Europe?
The next dates haven't been confirmed. The last edition we have on record was 21–22 Nov 2016.
Where is it held?
The last edition we have was at Dorint An Der Messe Basel, Basel, Switzerland.