Clinical Research Services That Deliver Impact
Solving All the Difficult Challenges Throughout the Clinical Development and Regulatory Approval Process.
Whether you are looking for a partner to support you throughout the entire clinical development process or just looking for additional expert functional support, Veristat can help you succeed.
We understand that all the easy challenges have been conquered in your development programs, so you need to overcome process and scientific unknowns. To give you an advantage, Veristat has assembled a team of scientific-minded experts adept at clinical trial planning and conduct, navigating the regulatory approval process and ensuring product safety of marketed products.
Explore Our Integrated Service Offerings
Discover how we help bring novel medical therapies through the clinical development lifecycle to market with confidence.
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.
Examine how we help you design, collect, analyze, convert and report your clinical trial data to the regulatory agencies.
Veristat recently expanded its pre-approval and post-marketing pharmacovigilance and safety surveillance expertise.