Ready to reduce your clinical development timelines and headaches?
Veristat can support your success across the entire drug development journey with scientific thinking and a proven versatile approach
Veristat is the science-first full-service CRO and consultancy offering a broad range of strategic consultancy and regulatory capabilities. We partner with sponsors to support their delivery of life-changing therapies to patients, helping them make sound decisions amidst uncertainty. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently.
With our focus on novel drug development and more than 29 years of experience, our versatile approach and scientific thinking make seemingly impossible challenges possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact.
The Science-First CRO. Veristat.
Your versatile full-service CRO integrating clinical planning and regulatory consulting expertise to help you rapidly advance your complex or novel therapies from strategy through execution.
From study start-up through study lock— Veristat experts design and run each clinical trial using tailored trial conduct/deployment and innovations.
- Flexible Delivery Models— consulting, full service and functional service/FSP.
- Multi-regional Clinical Trial Operations— patient recruitment, patient retention & site engagement, monitoring & site management and project management.
- Purpose-fit Clinical Trial Conduct— Decentralized Clinical Trials (DCTs), hybrid trials, adaptive and rescue trials, natural history, observational and real-world evidence studies.
- Harmonized Expertise— biometrics, medical affairs & safety, regulatory affairs, medical writing and IND/CTA maintenance.
We ensure a unified approach ideal for your target patient and study, augmenting your in-house team with vetted talent as needed. Speak to an expert today!
End-to-end regulatory registration support - planning, application preparation, and publishing.
- Regulatory Consulting — plan and implement regulatory strategies for successful interactions with the FDA, MHRA, EMA and other global regulatory agencies.
- Marketing Applications — navigate operationally complex submissions, overcome data analysis challenges and streamline the medical writing process.
- Regulatory Publishing —support the successful electronic submission of your regulatory documents.
- Regulatory Writing— tailor your regulatory documents to meet the specific requirements of the product, indication and regulatory agency.
From Phase 1 to MAA/BLA/NDA and beyond, Veristat’s world-class regulatory experts can help you advance your novel innovation through the regulatory approval process. Speak to an expert today!
Regulatory, Statistical, Clinical and Medical know-how throughout the entire clinical development and approval lifecycle.
- Clinical Development Program Planning—create your plan with the end game in mind.
- Clinical Trial Planning & Conduct—helping you navigate the transition from lab to clinic.
- Regulatory Strategy—plan and implement strategies for successful interactions with global regulatory bodies.
We partner with you to design and advance your programs with quality, speed and transparency. Speak to an expert today!
Ensure patient access and safety while managing risk getting— and keeping— your product on the market.
- Pharmacovigilance Consulting and Program Management— meet your regulatory requirements through sound processes and efficient systems.
- Market Access — implement reimbursement, healthcare compliance, public affairs & quality assurance solutions that scale to your evolving needs.
- Post Market Surveillance— support ongoing patient safety and product quality to safeguard your success.
Veristat supports your patients with difficult-to-treat diseases and conditions to live safely while helping your organization meet its goals. Speak to an expert today!
Ready to Learn More?
Put Veristat’s versatile approach and bold thinking tailored for every engagement to work for you. Schedule a no-obligation introductory call with us now.
