Registry Design & Implementation

Comprehensive services to meet all your Registry Design & Implementation needs

  • Common Data Element (CDE) and metadata driven Registry eSolution implementation
  • Development of Pilot Registry with core and focused data elements and data sets
  • Creation of data collection forms
  • Development of patient reported outcomes module

our Case Studies

Global Full service Clinical Trial Support to Assess Medical Device on Neurology Patients Including with Alzheimer’s Disease

Full Service Clinical Trial Operation, Monitoring, Safety and Data Management support for a First-in-Human Phase 1 Dose Escalation Oncology Study

Prospective Full-Service Medical Device Clinical Trial on patients with Persistent Post-Concussive Symptoms (PPCS) after Traumatic Brain Injury (TBI)

Personalized Study Support and Effective Study Initiation of a Global Multicenter Orphan Phase 3 Imaging Trial

We have supported several US federal agencies, including 10 NIH Institutes, CDC, and DoD for almost four decades with the coordination of hundreds of clinical trials and epidemiological studies in a wide variety of therapeutic areas
Neurology

Neurology

Infectious Disease

Infectious Disease

Musculoskeletal Conditions

Musculoskeletal Conditions

Oncology

Oncology

Key Therapeutic Areas

Expertise transcending disease areas to bring life saving medicines to market

30+ Years of Experience at Your Service

Clinical Trials

Clinical Trials

Medical Device Trials

Medical Device Trials

Registries

Registries

Observational Studies

Observational Studies

Reach Us Today

We know your projects are unique. You can rely on our team of specialized research methodologists to design and manage your program. Tell us what you need, and we will work with you to create a customized, flexible approach with pricing to meet the particular needs of your research program.