Register now for our next BlueReg Webinar:
October 14, 2021
12:30 PM EDT I 06:30 PM CEST I 05:30 PM BST
When dealing with promotional materials, companies have to face different practices and systems per country. This is important to understand especially for a new company launching its first medicinal product in the European Union.
The participants will learn about how to set-up launch of promotional materials from a Regulatory perspective with a specific focus on some European markets. This will include project kick-off, examples of country specific requirements, need for process mapping, up to the submission to authorities when applicable.
Importance and role of local representatives (Information Officer in Germany, Chief Pharmaceutical Officer in France…) and communication with local representatives and headquarter representatives will also be discussed.
Learn about launch set-up for promotional materials for companies targeting EU markets
Understand main regulatory differences in some EU markets
Apply this knowledge learned to their personal challenges in their organizations
Director Business Development & Account Management
Senior Consultant, Regulatory Affairs
We are an international pharma consultancy offering strategic regulatory advice and hands-on outsourcing solutions to life sciences companies through services ranging from product development to life cycle management, Early Access Programmes and more
We provide strategic and tailored solutions to our clients, from start-up to large life sciences companies, to support their ability to develop and offer healthcare products to patients.
We encourage motivation and development of our people through opportunities to learn in a supportive and positive environment.
BlueReg aims to contribute to a world where patients have better access to a variety of safe, effective healthcare products, and innovative treatments.