Scientific Expertise to Solve any Clinical Development Challenge

The right expertise for clinical program planning, trial conduct, navigating the regulatory approval process, and ensuring post-approval safety surveillance.

Veristat supported Marketing Applications for 10% of all FDA Novel Drug Approvals in 2020.

600+ Rare Disease Clinical Trials

110+ Marketing Applications Supported

30+ COVID-19 Programs

Expanding Clinical Trials to the US

Specialty Expertise

Our team of scientific experts is easy to work with, even for the rarest, most complex, and never done before novel therapies.

Cell & Gene Therapies

Decentralized Trials

All Services

Oncology

Infectious Disease

Marketing Application

Driving Success

I am grateful for the dedication, excitement and clinical trial expertise that the Veristat team provided for our program. Veristat's collaboration was critical to the successful clinical trials that led to our product's approval.

President of Research of Development

Mid-Size Pharma

Counting on Veristat for the preparation of our New Drug Application (NDA) is the culmination of years of hard work and dedication by the Veristat team. I have truly come to rely on the clinical and statistical expertise of Veristat over the past decade.

Chief Executive Officer

Mid-Size Pharma

I wanted to let you know the protocol has been fully approved and is now considered final. We could not have done this without you, and we are grateful for your significant contributions.

Head of Regulatory & Medical Writing

Small Pharma

Thank you Veristat for your close collaboration and attentiveness during our virtual inspection with the Japan PMDA. They have no further questions at this point about our jNDA.

Sr Director of Statistical Programming

Mid-Size Biopharmaceutical

Let me express my gratitude to the Veristat team for publishing our MAA…67 days from database lock to filing! This is quite an accomplishment. It has truly been a privilege to work with Veristat on this important milestone for our patients.

Director, Regulatory Operations

Clinical Stage Biopharmaceutical

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