Clinical Trial Shared Resource
IRB administrative requirements, adverse event reporting and trials information and referral.
What they do
- Services
- IRB administrative requirements
- Adverse event reporting
- Trials information and referral
- Consent and eligibility forms
- Protocol file repository
- Clinical research personnel assignment
- Experimental drug regulation
- Trials design and implementation
- Regulatory requirements
- Statistics review
- Budget review
- Industry contracts review
- Phase I and II study design
- Study monitoring
- Patient care follow-up
- Clinical research translation