About Us

Veristat is a smart, effective and impactful CRO that will help you advance your medical therapies through the clinical development and regulatory submission process. Ultimately, we partner with and guide our clients to market success so that their therapies become available to improve and save people’s lives.  

Partnering with Emerging, Small & Mid-Size Biopharma

We focus on providing effective strategies and impactful solutions to ensure the success of your early phase studies.  Regardless of your end goal, we’ll be your TRUE partner and lead you down the right path towards success.  

Veristat is committed to building TRUE Partnerships with our clients.   For many of our clients, we literally become your project team, and for others, we provide the medical, scientific, clinical and statistical expertise to help you advance your therapy into and through clinical development.   

At Veristat, building TRUE Partnerships with our clients is what makes us successful.

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CRO Focused on Emerging, Small & Mid-size Biopharmaceuticals

  A TRUE Partnership is built upon a foundation of: 

  • Trust through transparency
  • Respect of culture
  • Understanding of goals and expectations
  • Evolving for change

 

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Partnering Throughout the Clinical Trial &  Approval Process

The Leader In Strategic Clinical Development Decision-Making

Making decisions at the right time based on the right information is critical to a clinical development program's success.   Untimely or poor decisions can throw a clinical trial off track.  For nearly 25 years, Veristat has been a trusted source of intellectual leadership and guidance in clinical development.  We provide strategic level thinking to help clients optimize their clinical development approaches, trial designs and regulatory submission strategies.

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Unrivaled Regulatory Submission Knowledge

Integrated Veristat teams have  performed over 75 Regulatory submission projects that led to more than 50 regulatory approvals to date. 

Veristat is proud to be a part of this many regulatory successes!   While we can’t claim credit for developing these new products, we helped along the way and executed a flawless regulatory submission process which helped lead to the successful approval of these life-changing and life-saving products.   Our project managers, medical writers, data managers, data standards team, biostatisticians and statistical programmers work tirelessly in unison to prepare regulatory submissions. In the end, there are millions of people whose lives have been improved or saved due to these approved treatment options.

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Full service CRO

 

 

Experts In Integrated Clinical Trial Execution -

From Start To Finish

 Veristat will collaborate with you to provide the operational, scientific, functional and/or therapeutic expertise required to conduct your clinical trial from start to finish.   We can project manage every aspect of your trial or just provide supplemental services to round out your team.  Our experts collaborate with you by providing strategic consultation throughout your program, clinical operations support, safety management, data management, CDISC implementation, biostatistics, statistical programming, medical writing and regulatory submissions support.

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Therapeutic Centers Of Excellence

Our global team of scientific, operational, medical and regulatory experts apply knowledge and experience across broad range of therapeutic areas to solve your toughest drug development challenges

Veristat is committed to partnering with you to bring life-enhancing, life-extending and life-saving therapies to market.    Our experience spans nearly every therapeutic area.   We are currently working on many projects to treat Cancers, Rare Diseases, Neurological Disorders, Infectious Diseases and more. Many of these treatments are vaccines, biosimilars, gene therapies, complex generics, immuno-therapies and novel drugs.

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