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Veristat is a full-service CRO that helps life sciences companies design, run, and submit clinical trials.
Veristat is a full-service contract research organization (CRO) that partners with life sciences companies to design, run, and submit clinical trials. It provides strategic consulting, regulatory affairs, clinical operations, medical affairs, biometrics, pharmacovigilance, and regulatory publishing, along with resourcing, through full-service trial planning, conduct, and regulatory submission capabilities. With a global reach and activity across multiple therapeutic areas, Veristat supports end-to-end clinical research programs.
Mission statement
To enable life sciences companies to bring therapies to patients faster by delivering high-quality, collaborative, full-service clinical research solutions.
Products & Services
Full Service Solutions Solution
Comprehensive clinical development support for successful trial execution.
www.veristat.com/services/full-service-solutions- ✓ Clinical Trial Conduct — Execute Clinical Trials
- ✓ Regulatory Submission — Submit Regulatory Documents
- ✓ Clinical Trial Planning — Plan Clinical Trials
- ✓ Data Monitoring and Safety — Monitor Data and Safety
- ✓ Patient Recruitment — Recruit Patients Effectively
Decentralized Trials Solution
Streamline clinical trials with our comprehensive decentralized solution.
www.veristat.com/decentralizedclinicaltrials- ✓ Remote Patient Monitoring — Enhances Patient Engagement
- ✓ Decentralized Recruitment — Increases Trial Access
- ✓ Regulatory Compliance Support — Ensures Compliance
- ✓ Data Integration and Analytics — Improves Data Accuracy
Rescue Trials Solution
Enhance ongoing clinical studies through targeted rescue trial solutions.
www.veristat.com/clinical-trial-rescue-programs- ✓ Trial Optimization — Enhance Efficiency
- ✓ Regulatory Guidance — Ensure Compliance
- ✓ Patient Recruitment Strategies — Increase Enrollment
- ✓ Data Analysis Support — Maximize Insights
Natural History Trials Solution
Gain insights into disease progression to enhance trial design.
www.veristat.com/solutions/natural-history-studies- ✓ Disease Progression Characterization — Understand Disease Dynamics
- ✓ Informed Trial Design — Enhance Clinical Trials
- ✓ Support for Regulatory Submission — Facilitate Regulatory Approval
Strategic Consulting Service
Enhance trial success with expert strategic consulting services.
www.veristat.com/services/strategic-consulting- ✓ Statistical Power — Ensure Study Power
- ✓ Adaptive Design — Enhance Study Flexibility
Regulatory Affairs Service
Comprehensive regulatory services to ensure compliance and successful submissions.
www.veristat.com/services/regulatory-affairs-overview- ✓ Regulatory Consulting — Optimizes Program and Trial Design
- ✓ CMC (Chemistry, Manufacturing, and Controls) — Ensures Compliance with CMC Standards
- ✓ Marketing Applications — Navigates the Marketing Application Process
- ✓ Agency Meetings — Facilitates Effective Communication
- ✓ Medical Devices/IVDs — Specialized Support for Devices
- ✓ Medical Writing — Produces High-Quality Regulatory Documents
- ✓ Regulatory Publishing — Streamlines Documentation Submission
Clinical Operations Service
Streamline clinical trials with expert management and patient engagement.
www.veristat.com/services/clinical-operations- ✓ Patient Recruitment — Maximize Participant Enrollment
- ✓ Monitoring & Site Management — Ensure Trial Compliance
- ✓ Project Management — Coordinate Trial Activities
- ✓ Patient Retention & Site Engagement — Enhance Participant Retention
Medical Affairs Service
Enhances clinical trial integrity through comprehensive medical support and safety processes.
www.veristat.com/medical-affairs-overview- ✓ Clinical Trial Safety — Ensures Trial Safety
- ✓ Data Monitoring Committees — Facilitates Oversight
- ✓ Medical Monitoring — Oversees Medical Aspects
- ✓ Pharmacovigilance — Monitors Drug Safety
Biometrics Service
Comprehensive biometrics services for managing clinical trial data and analyses.
www.veristat.com/services/biometrics- ✓ Data Management — Streamline Data Processes
- ✓ Biostatistics — Enhance Data Interpretation
- ✓ Statistical Programming — Automate Data Analyses
- ✓ Data Monitoring Committees — Ensure Trial Integrity
- ✓ Standards Implementation — Align with Regulatory Standards
Pharmacovigilance Service
Ensure patient safety and regulatory compliance through comprehensive pharmacovigilance services.
www.veristat.com/pharmacovigilance- ✓ Safety Monitoring — Track Adverse Events
- ✓ Regulatory Compliance Support — Ensure Regulatory Adherence
- ✓ Integrated Data Management — Optimize Data Handling
Strategic Resourcing Service
Enhances clinical trial efficiency with tailored staffing solutions.
www.veristat.com/services/strategic-resourcing- ✓ Flexible Staffing Solutions — Optimize Staffing Levels
- ✓ Expert Clinical Personnel — Leverage Expert Knowledge
- ✓ Customized Resource Plans — Receive Tailored Solutions
Market Segments
End-to-end clinical development
Comprehensive management of clinical programs from protocol design through execution and regulatory submission to deliver complete development programs.
Clinical operations and site management
Operational services for trial conduct including project management, site monitoring, site management, patient recruitment and retention.
Decentralized clinical trials
Planning and execution of decentralized and hybrid trials including remote patient monitoring, decentralized recruitment, and multi-source data integration.
Biometrics, data management and statistical programming
Biostatistics, statistical programming, clinical data management, standards implementation and data monitoring committee support for analysis-ready datasets.
Pharmacovigilance and medical monitoring
Safety surveillance, adverse event reporting, pharmacovigilance, medical monitoring and data monitoring committee support to manage patient risk.
Regulatory affairs and submission support
Regulatory strategy, agency interactions, CMC and marketing application preparation, regulatory publishing and submission management.
Natural history and disease characterization
Natural history studies and disease progression characterization to inform trial design, endpoints and regulatory filings, commonly used in rare disease programs.
Clinical trial rescue and remediation
Remediation and optimization of underperforming trials through data analysis, recruitment interventions, regulatory guidance and operational redesign.
Strategic resourcing and staffing
Flexible staffing, customized resource plans and access to expert clinical personnel to scale trial teams and close capability gaps.
Clinical trial design and adaptive methods
Statistical and design consulting including adaptive design, power calculations and design optimization to improve trial efficiency and decision making.
Common Questions
- What does Veristat do?
- Veristat is a full-service contract research organization (CRO) that partners with life sciences companies to design, run, and submit clinical trials. It provides strategic consulting, regulatory affairs, clinical operations, medical affairs, biometrics, pharmacovigilance, and regulatory publishing, along with resourcing, through full-service trial planning, conduct, and regulatory submission capabilities. With a global reach and activity across multiple therapeutic areas, Veristat supports end-to-end clinical research programs.
- What is Veristat's role in the End-to-end clinical development market?
- Comprehensive management of clinical programs from protocol design through execution and regulatory submission to deliver complete development programs.
- What is Veristat's role in the Clinical operations and site management market?
- Operational services for trial conduct including project management, site monitoring, site management, patient recruitment and retention.
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