• 9: Careers
• 10: Management
• 11: Contact
• 12: History

• 3: CRO Activities
• 4: Professional Services
  • 4.1: Statistical
  • 4.2: Regulatory
  • 4.3: Monitoring
  • 4.4: Biorepository Management
  • 4.5: Data Management
  • 4.6: SDTM Data Conversion
  • 4.7: SDTM Data Conversion Classes
• 5: Trial Management Software
• 6: Resources
• 7: Projects
  • 7.1: Current Projects
  • 7.2: Past Projects of Note
  • 7.3: Select Publications
• 8: Clients/Partners
• 13: News

C-TASC Clinical Trials & Surveys Corporation

The Difference Is in the Details

It all begins with something we have stood for since C-TASC opened its doors over 20 years ago—results. Results that break through the obstacles to make study data more relevant, more reliable—more undeniable.

By providing our dedicated clients with proven products and services, we ensure the safe and efficient management of:

• Clinical trials
• Clinical surveys
  
• Case/control studies
  
• Clinical registries
  
• Clinical cohort studies
  
• Laboratory studies
  

The C-TASC team is comprised of a diverse group of talented individuals working together to ensure that each and every job undertaken is completed according to industry standards.

As a group, we approach each and every project as if it were our only project…asking questions, questioning answers, and thoroughly analyzing anything and everything that comes before us.

The Rules are Changing and So Must the Solutions

Security and peace of mind are critical components to everything we do. C-TASC’s software group has developed, hosted, and managed Web-based clinical data management systems for numerous studies.

Our proprietary software-as-a-service (SaaS) product—StudyCTMS—is an end-to-end clinical trials management system that features electronic data capture (EDC), integrated statistical analyses using SAS, a “drag & drop” form builder utility, and many other intuitive tools to guarantee fast and reliable results. These are just a few of the advanced and continually evolving features that make StudyCTMS an attractive and affordable solution for any investigator.

C-TASC’s experienced staff is also available to assist researchers with FDA-mandated Study Data Tabulation Model (SDTM) conversion. Our FDA-acceptable CDISC SDTM format conversion tool saves researchers time and money when preparing materials to be submitted for regulatory review.

Current C-TASC News