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Services And Support For Existing Research Sites

NCR provides trial management and consulting services for existing Research Sites that might need assistance with specific tasks. We work with them to find a timeline and budget that fits your needs.

  • Help in site feasibilities
  • Full Coordinator support for the duration of the study
  • Trainings at reasonable costs
  • ICH/GCP trainings for Coordinators and Principal Investigators
  • Source document preparations/ Contract and budget negotiations
  • Help in Sponsor/ FDA Audits
  • Regulatory document preparations and submissions on your behalf
  • We help you getting new trials to your site for your qualified physicians
  • Offer back up coordinator services for your primary coordinators
  • IRB submission
  • Regulatory Document submissions

We also help and support to get you awarded with the new clinical trial, you can have us manage it or you can choose to do it on your own

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