All BioPartners studies undergo review and approval by an Independent Review Board (IRB) before initiation.
IRB oversight ensures:
- Ethical conduct of research
- Protection of participant rights and welfare
- Accuracy and transparency of the Informed Consent Form (ICF)
- Compliance with federal regulations and ethical guidelines
We collaborate with well-established central IRBs, enabling fast turnaround times and rapid activation.
Ongoing responsibilities include:
- Continuing reviews
- Reporting of AEs, SAEs, and protocol deviations
- Amendment submissions
Continuous ethical oversight throughout the study