The Potential for New Efficiencies to Allow for Scalability in Cell and Gene Therapy Clinical Development
2021 TOPRA Awards Event
July 27, 2021
Veristat To Sponsor the TOPRA Awards 2021
London - UK 18th November 2021
Orphan Drug Congress Europe | Booth #54
July 9, 2021
Meet Veristat at the Orphan Drug Congress 2021 taking place on 15-18 November 2021, Booth #54
On-Demand Webinar| Expanding your Clinical Trial into the US - Submit your IND for non-US Sponsors
May 20, 2021
How, why, and when to expand your clinical trial program into the US, including differences between IND and CTA
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
Veristat experts recently led an Xtalks webinar on lessons learned for planning decentralized clinical trials.
Gene Therapy for Rare Disorders 2021
January 22, 2021
Meet Veristat at the Virtual event taking place 23-24 February 2021
Webinar | Roadmap to Market for Cell and Gene Therapies
October 12, 2020
View the On-Demand Webinar
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.
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.