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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