How it works
Eligibility Requirements
Clinics and providers should meet the following criteria:
- Licensed medical professional or certified research facility
- Active practice focused on targeted indications
- Ability to perform required procedures (IV, IM, IA, PAI, IN)
- Willingness to share de-identified patient data
- Commitment to following study protocols
How It Works
Submit Application
Clinic completes registration and eligibility screening.
Approval & Onboarding
CSR verifies credentials and confirms study capabilities.
Receive Protocols
Providers receive study guidelines, procedures, and documentation.
Conduct Investigations
Medical teams perform studies following predetermined protocols.
Share De-Identified Data
Providers upload structured data securely to CSR.
Collaborate & Contribute
Collected outcomes help improve devices, therapies, and patient care.
FAQs
Are these paid studies?
Often not; participation supports scientific progress and may offer access to new treatments.
Do we need IRB approval?
CSR focuses on informal studies using standard-of-care treatments where IRB oversight is typically not required.
How long does approval take?
Most applications are reviewed within several business days.