2 min read
FDA Prior Knowledge Guidance: A New Framework for Natural History Evidence
June 22, 2026
What the FDA's prior knowledge guidance means for natural history evidence and shared datasets
On June 2,...
1 min read
As Veristat has just passed its first year anniversary in the UK, we are excited to exhibit for the first time at Outsourcing in Clinical Trials UK & Ireland 2017.
Join Veristat and clinical trial partners to discuss how the backdrop of shifting priorities and uncertain political climate are disrupting and changing clinical trial operations both today and moving forward.
Key discussion topics will include:
- Tackling the Evolving Political and Regulatory Landscape in the UK: Brexit, EMA, ICH Guidelines & More
- The New EU Clinical Trials Regulation: As it becomes the law in 2018, are you prepared for its impact to drug development in the EU?
- Risk Based Monitoring & Targeted SDV: Advice for successfully implementing risk based monitoring
- Managing Your CRO for Competitive Advantage
- What Does Effective Communication Look Like When Managing Established CRO Partners
Visit Veristat at Booth #15
Visit the Veristat booth #15 to meet our team and learn how why we should be your clinical development and regulatory submission partner. Our teams will help design and implement the clinical and biometrics components of your clinical trial and will help you prepare your regulatory submissions.