BlueReg Webinar:

Regulatory compliance: How to accelerate your medicinal product launch in Europe?

28 April 2021

11AM EDT I 4PM BST I 5PM CEST

  • This webinar will focus on the design of the regulatory strategy to prepare the launch sequence for your first medicinal product in Europe. 

  • We will also present the coordination and the set-up of a tailored outsourcing regulatory platform to comply with the EU & local requirements.

 

What will you learn?

Essential regulatory requirements to address for your medicinal product launch.

How to structure your regulatory team for your launch.

How to set up your regulatory launch priorities.

Our speakers

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Anne- Valérie Faucher

Associate Director, Regulatory Affairs

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Nadia Boehringer

Vice-President, Global Head Regulatory & Scientific Affairs

Who we are?

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

What is our mission?

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.

For what world?

BlueReg aims to contribute to a world where patients have better access to a variety of safe, effective healthcare products, and innovative treatments.

For more information contact us or visit our website

 

contact@blue-reg.com

www.blue-reg.com