Navigating the Patient Experience When Pivoting to a Virtual Model Mid-Study
Webinar | Strategies for Solving the Challenges of an Extraordinary Natural History Study
May 16, 2022
Regulatory Pathways Available to Speed Development and Approval
Webinar on Medical Devices Software
January 26, 2022
Veristat (formerly DDR) and partner CN Group co-organized an informative session on the development and Regulation of Medical Device Software (MDSW). The live webinar was held on 14 October 2021 and covered the main considerations to keep in mind when developing a MDSW under the new Medical Devices Regulation (MDR).
The Potential for New Efficiencies to Allow for Scalability in Cell and Gene Therapy Clinical Development
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.
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.