Events and Conferences

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Executive Roundtable Meeting | Decentralized Trial Solutions for Complex Clinical Trials

January 13, 2023

Share your experiences and learn from other

industry executives


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Pharmacovigilance  Webinar  |            Save the date

September 2, 2022

Coming Soon!


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On-Demand Webinar  | Future Trends on European Regulations on Medicines

September 2, 2022

Veristat and TOPRA hosted a webinar on the topic:                    Future Trends on European Regulations on Medicines                            


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Webinar | Orphan Drug Designation

August 29, 2022

Orphan Drug Designation - The Considerations, The Rewards, and How They Differ Between The US and Europe 


Recording available now!


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Webinar | Decentralized Trial Solutions for Complex Clinical Trials

July 7, 2022

Improving the patient experience while overcoming DCT challenges for a pediatric rare disease population


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Webinar | Strategies for Solving the Challenges of an Extraordinary Natural History Study

May 16, 2022

Navigating the Patient Experience When Pivoting to a Virtual Model Mid-Study


On-Demand Webinar

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On-Demand Webinar | What's New in Draft MHPD Guidance on Reporting Adverse Reactions for Marketed Products

April 12, 2021

Certus PV, a Veristat Company experts recently lead an Xtalks webinar - View it On-Demand Now

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On-Demand Webinar | How to Better Plan Your Decentralized/Virtual Clinical Trial

March 2, 2021

Veristat experts recently led an Xtalks webinar on lessons learned for planning decentralized clinical trials.

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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

View Webinar On-Demand


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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