Meet Our Team
Guy Shipman
Practice Lead | Regulatory Affairs
- Location UK & Europe
- Date Joined 09/07/2024
- Team UK & Europe
Since 2019, I've been a trusted advisor to Biopharma, Pharma, Biotech, and Medical Device companies, helping them navigate the complexities of Regulatory Affairs. I have a deep understanding of the entire regulatory landscape, from Clinical Development and CMC (including authoring) to Operations, Labeling, Lifecycle Management, Registrations (MAA, BLA, NDA), Compliance, and Medical Device Regulations (MDR, IVDR).
Previously, I specialised in connecting companies with top-tier contract Regulatory Affairs professionals in the UK and EU. Now, at Warman O'Brien, I'm thrilled to expand my reach and assist you in finding both Contract and Permanent talent for your Regulatory Affairs needs.