Markets we serve
We work across the U.S. life sciences market, with a focus on biotech, pharma, and medtech companies. Our specialist areas are regulatory affairs and pharmacovigilance.
Regulatory Affairs
Regulatory affairs is the function that guides a life sciences product through FDA requirements from early development to approval and beyond. For U.S. companies, it is essential because the FDA’s framework determines whether a product can be studied, approved, and sold.
We’ve built a niche within regulatory affairs to help biotech, pharmaceutical, and medtech companies move efficiently through the FDA process, reduce regulatory risk, and accelerate product development.
VP, Director & Head of Regulatory Affairs
Regulatory Affairs Associate & Officer
Senior Regulatory Affairs Specialist & Manager
CMC Regulatory Affairs Specialist
Regulatory Submissions Manager
Labelling & Artwork Regulatory Specialist
Regulatory Compliance Consultant
Regulatory Project Manager
Pharmacovigilance
PV (Pharmacovigilance) is the science and practice of identifying, evaluating, and preventing adverse effects and other drug-related problems. Our focus is on supporting life sciences companies with safety oversight, regulatory compliance, and lifecycle risk management in the U.S. market.
We’ve chosen to build a niche within PV because it is a critical function that protects patients, supports regulatory compliance, and helps life sciences companies manage product safety throughout the full product lifecycle.
Senior VP / VP / Director of Pharmacovigilance
PV Assistant / PV Administrator
Drug Safety Associate / PV Associate
PV Scientist / Safety Surveillance Scientist
PV Signal Detection Specialist / Risk Management Specialist
PV Compliance Specialist
Aggregate Reports Writer
PV Operations Manager / PV Project Manager
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