SQN is Now Veristat
As Veristat, we can help you overcome all the difficult challenges that arise during clinical development, regulatory approval, and post-marketing surveillance. There is no "one size fits all" approach to clinical research. Our teams partner with you to understand your goals to plan and execute your clinical program to achieve success.
Explore Our Integrated Service Offerings
Examine how we help you design, collect, analyze, convert and report your clinical trial data to the regulatory agencies.
Learn how Veristat’s expert consultants provide strategic as well as tactical decision making throughout the design and implementation of your clinical development program.
Discover how our teams partner and drive the project management, project administration, and clinical monitoring functions for your clinical trials.
Medical Affairs & Patient Safety
Learn how we plan and implement every clinical trial and program centered around patient safety and mitigating risks.
Learn how we write clinical trial documents, regulatory agency communications, and marketing applications.
Veristat recently expanded its pre-approval and post-marketing pharmacovigilance and safety surveillance expertise.