Vice President, Regulatory Affairs
- European Registration procedures
- Development (CTA, PIP, ODD, SA)
- Project management
Peggy has a significant experience in European Regulatory Affairs gained through more than 15 years of working within the pharmaceutical industry or consultancy company, and including more than 10 years in regulatory Affairs drug development and registration in Europe.
Prior to joining BlueReg Pharma Consulting, Peggy was at Allergan SAS, where her most recent role was Regulatory manager in charge of European Clinical trials initiation and maintenance in Urology and Neurology. She also participates to the development of internal procedures, templates and tools in order to harmonise clinical trials management within Allergan.
In this role she was also involved in European registration procedures (MRP and CP) in ophthalmology and neurology and responsible for the maintenance of a products portfolio in neurology and ophthalmology for Europe.
When she moved to Consultancy she had the opportunity to work on various development projects requiring a regulatory strategy input such as European scientific advice, paediatric investigational plan, orphan drug designation, as well as on several registration procedures.