Instat Clinical Research
Clinical research organization and consultancy providing integrated, full‑service clinical development, biometrics, regulatory, safety, and medical writing services to support regulatory registration and commercialization across the product lifecycle. The page also confirms the integration of an acquired biometrics-focused team into the organization to expand analytics capabilities.
Industries
Nr. of Employees
small (1-50)
Products
Full-Service Clinical Trials
Advance your trials through all phases with a trusted partner offering full-service support.
Strategic Consulting
Strategic guidance to hit your clinical and regulatory milestones across the entire development journey.
Biometrics
Examine how we help you collect, analyze, convert, and report your clinical trial data to the regulatory agencies.
Medical/Regulatory Writing
Learn how we write clinical trial documents, regulatory agency communications, and marketing applications.
Data Monitoring Committees
Improve patient safety and reduce risks with proven and acceptable independent DMC models and administration best practices.
Regulatory Affairs
Apply our regulatory expertise and strategy throughout all phases of clinical development into commercialization.
Full-Service Clinical Trials
Advance your trials through all phases with a trusted partner offering full-service support.
Strategic Consulting
Strategic guidance to hit your clinical and regulatory milestones across the entire development journey.
Biometrics
Examine how we help you collect, analyze, convert, and report your clinical trial data to the regulatory agencies.
Medical/Regulatory Writing
Learn how we write clinical trial documents, regulatory agency communications, and marketing applications.
Data Monitoring Committees
Improve patient safety and reduce risks with proven and acceptable independent DMC models and administration best practices.
Regulatory Affairs
Apply our regulatory expertise and strategy throughout all phases of clinical development into commercialization.
Services
Outsourced study operations and program management for clinical trials across phases.
Regulatory and development strategy to meet clinical and registration milestones.
Data collection, conversion, analysis, and reporting to support regulatory submissions.
Preparation of regulatory documentation and clinical writing for agency communications and marketing applications.
Safety surveillance and patient safety management across the product lifecycle.
Flexible resourcing and staffing solutions to augment sponsor teams and meet program milestones.
Outsourced study operations and program management for clinical trials across phases.
Regulatory and development strategy to meet clinical and registration milestones.
Data collection, conversion, analysis, and reporting to support regulatory submissions.
Preparation of regulatory documentation and clinical writing for agency communications and marketing applications.
Safety surveillance and patient safety management across the product lifecycle.
Flexible resourcing and staffing solutions to augment sponsor teams and meet program milestones.
Expertise Areas
- Clinical trial management
- Biostatistics and biometrics
- Regulatory strategy and submissions
- Pharmacovigilance and safety surveillance
Key Technologies
- Statistical analysis and biometrics
- Clinical data management systems
- Safety surveillance and pharmacovigilance systems
- Regulatory submission document workflows