Veronica Farrell-Lecomte's Location
United Kingdom
Veronica Farrell-Lecomte's Work
- Head of Regulatory Affairs Development Products @ GE HealthCare
- Director of Regulatory Affairs @ Kyowa Pharmaceutical, Inc.
- Director Global Regulatory Affairs @ Quintiles
- Senior Director Regulatory Affairs @ Novella Clinical
- Regulatory Consultant @ Freelance
- Director Reg Affairs (EMEA) @ PPD
- Director Reg Affairs @ PRA Health Sciences
Veronica Farrell-Lecomte's Skills
- Clinical Trials
- CRO
- Regulatory Submissions
- Biotechnology
- Regulatory Affairs
- Therapeutic Areas
- Sop
- Medical Devices
- Clinical Development
- GCP
Veronica Farrell-Lecomte's Summary
Veronica Farrell-Lecomte, based in United Kingdom, is currently a Head of Regulatory Affairs Development Products at GE Healthcare, bringing experience from previous roles at Kyowa Pharmaceutical, Inc., Quintiles, Novella Clinical, Inc. and Freelance. With a robust skill set that includes Clinical Trials, CRO, Regulatory Submissions, Biotechnology, Regulatory Affairs and more, Veronica Farrell-Lecomte contributes valuable insights to the industry. Veronica Farrell-Lecomte has 5 emails on RocketReach.
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