Events and Conferences

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Gene Therapy for Rare Disorders 2021

January 22, 2021

Meet Veristat at the Virtual event taking place 23-24 February 2021

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Webinar | Roadmap to Market for Cell and Gene Therapies

October 12, 2020

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Nothing is standard about the study design, study conduct or the regulatory process in cell and gene therapy trials. Every cell and gene therapy is different due to the specific characteristics of each product, with a complicated regulatory approval process and unique therapeutic challenges.

 

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Webinar | Reducing Study Build Time from Weeks to Days

October 1, 2020

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Study start-up and post-go-live protocol amendments can be lengthy, costly, and disruptive to a clinical trial. But with the right technology, data managers can accelerate timelines and overcome these challenges.

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Cell and Gene Meeting On The Mesa

August 3, 2020

Meet Veristat at the Virtual event taking place October 12-14, 2020.

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Gene Therapy for Rare Disorders Europe

August 3, 2020

Meet Veristat at the Virtual event taking place 26-28 October 2020.

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Webinar | Minimize Disruption of Your Oncology Trial

June 4, 2020

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As the world begins to relax restrictions, what are the lessons learned that can catapult us into the next innovation in trial operations for good? 
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Webinar | Are you Ready to Begin Planning your IND Submission?

April 13, 2020

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Submitting an Investigational New Drug (IND) application to the US FDA is a significant step in the development of a new drug or biologic product. But, are you ready? 
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Clinical Trials Europe 2019 | Formerly PCT Europe

October 24, 2019

Veristat will be attending Clinical Trials Europe 2019,  the conference formerly known as the Partnerships in Clinical Trial Europe conference, for the first time this year.  

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Evolution Summit Boston | Managing Risk in Clinical Trials for E6 (R2) Compliance

October 11, 2019

Are your risk-management strategies for clinical trials E6 (R2) Compliant?     Learn how to be sure.   

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Webinar | A Patient-Centric Approach to Clinical Trial Recruitment & Retention

October 3, 2019

Webinar Summary

Patient recruitment continues to be the number one reason for study delays. It is estimated for every day a drug is not on the market, $1 million USD is lost in revenue, and more importantly, patients suffering from illnesses are left waiting for products that can help them achieve their health goals or provide a better quality of life.
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