SQN Clinical
Veristat is a science-first full-service CRO and consultancy with over 29 years of experience, dedicated to supporting the development and approval of complex and novel therapies. They offer a versatile approach, integrating clinical planning, regulatory consulting, and scientific expertise to help sponsors accelerate their drug development journey, from strategy through execution, ensuring safety, efficacy, and regulatory success.
Industries
Nr. of Employees
medium (51-250)
SQN Clinical
Products
Resource library (webinars, case studies, fact sheets, blogs)
Collection of educational and technical resources including webinars, case studies, fact sheets and blog articles on clinical development topics.
Resource library (webinars, case studies, fact sheets, blogs)
Collection of educational and technical resources including webinars, case studies, fact sheets and blog articles on clinical development topics.
Services
End-to-end clinical trial execution from study start-up through database lock and clinical study report, including multi-regional operations and monitoring.
Interdisciplinary trial planning including protocol development, population selection, control selection, outcome measures and regulatory-aligned development plans.
Regulatory strategy, preparation of marketing applications and electronic publishing support for interactions with global regulatory agencies.
Biostatistical planning, adaptive design implementation, Bayesian dose-escalation strategies, simulations and statistical programming support.
Clinical data capture strategy, EDC build/test/deploy, integration of ePRO/eSource/eConsent, data cleaning, and implementation of clinical data standards to support regulatory reporting and analysis.
Design and delivery of decentralized trial ecosystems including at-home visits, traveling nurse dosing, telemedicine, remote data collection and logistics.
End-to-end clinical trial execution from study start-up through database lock and clinical study report, including multi-regional operations and monitoring.
Interdisciplinary trial planning including protocol development, population selection, control selection, outcome measures and regulatory-aligned development plans.
Regulatory strategy, preparation of marketing applications and electronic publishing support for interactions with global regulatory agencies.
Biostatistical planning, adaptive design implementation, Bayesian dose-escalation strategies, simulations and statistical programming support.
Clinical data capture strategy, EDC build/test/deploy, integration of ePRO/eSource/eConsent, data cleaning, and implementation of clinical data standards to support regulatory reporting and analysis.
Design and delivery of decentralized trial ecosystems including at-home visits, traveling nurse dosing, telemedicine, remote data collection and logistics.
Expertise Areas
- Clinical trial management
- Regulatory strategy and submissions
- Biostatistics and statistical programming
- Decentralized and hybrid clinical trials
Key Technologies
- Electronic data capture (EDC) systems and clinical database deployment
- ePRO (electronic patient-reported outcomes)
- eSource
- eConsent
News & Updates
Webinar on strategies to accelerate patient-centric trials.
Participation in the 2025 ASCO meeting in Chicago.
Event in Pennsylvania in May 2025.
Event in Basel, Switzerland, in May 2025.
Event in Washington D.C. in April 2025.
Analysis of recent FDA delays and their impact on biotech development strategies.
Webinar on strategies to accelerate patient-centric trials.
Participation in the 2025 ASCO meeting in Chicago.
Event in Pennsylvania in May 2025.
Event in Basel, Switzerland, in May 2025.
Event in Washington D.C. in April 2025.
Analysis of recent FDA delays and their impact on biotech development strategies.