Resources and Services

CRRF provides the following services:

Clinical Research Protocol Development
Feasibility Assessment
Consent development
Collection of regulatory documents
Investigational Device Exemption/Investigational New Drug Support
IRB Submission
Contract and/or Budget Negotiations
Credentialing Study Staff
Office of Sponsored Programs Processes
Patient Recruitment
Safety Reporting
Data Collection/Entry
Study Visit & Procedure Completion/Coordination
Specimen Collection
Shipping or Delivery to Core/Central Lab
Collaborator/Mentor matching in projects involving occupational pulmonary disease