This is the must-attend training course for anyone needing to learn the essentials of European Regulatory Affairs - it has been extended to two days to include more topics, and it is kept up to date in minute detail by the experienced faculty.
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. In addition the specific European procedures for orphan drugs, paediatrics, advanced therapies and combination products will be discussed. This will cover the different steps and timelines in the different procedures, the clock-stops, the compiling of questions etc.
An introduction regarding the lifecycle will be given by information in respect to pharmacovigilance, variations and renewals.
The course will cover the curernt registration systems available for approval of 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
Decentralised procedure and referrals
What the participants from previous courses say:
"The very well organized training course, at the high professional level."
"It helped a lot in understanding of European regulatory affairs as I have never worked with them before"
"I was pleased with attend to this course"
What You Will Learn
Who Should Attend
Professionals in regulatory affairs, project management and product development.
At the conclusion of this course, participants should be able to:
Explain the European Network and registration procedures
Describe the concepts of marketing authorisation and regulatory data protection
Discuss the key issues that impact the choice of the registration procedure
Describe the lifecycle management
Participants will complete a knowledge check at the end of the course and will be provided with feedback to ensure learning objectives are attained.
Hotel & Travel
DIA has blocked a limited number of rooms at the following hotel:
Hotel Novotel Paris Charenton
3-5 place des Marseillais
94227 CHARENTON LE PONT
at the rates of EUR 150.00 per room inclusive of breakfast and exclusive of VAT.
To make your reservation please use the hotel booking form.
Important: The room rate is available until 22 September 2014 or until the group block is sold-out, whichever comes first.
In case of cancellation: The room can be cancelled 43 hours prior arrival, after that the credit card will be charged for the 1st night.
The Hotel Novotel Paris Charenton is located 10 minutes from Gare de Lyon train station, the vibrant Bastille district & Bercy. The liberté metro station (line 8) opposite the hotel gives direct access to Paris's main attractions like Place de la Concorde, Eiffel Tower, Opéra, etc.
DIA Europe, Middle East and Africa
Phone.: +41 61 225 51 51
Fax: +41 61 225 51 52
Monday-Friday 8:00-17:00 CET
Agenda and Event Logistics
Gunta Sveke, Event Manager
Phone: +41 61 225 51 55