Prepare your study for ethics review.
BeaconCR organizes the documentation, language, and workflows an IRB or ethics committee expects to see. Final approval comes from an appropriately constituted IRB — we get you ready for that conversation.
What we do
- Protocol summaries and study design write-ups
- Informed consent language
- Parental permission and assent language when minors are involved
- HIPAA authorization language
- Recruitment and screening materials
- Investigator information and CV summaries
- Risk and benefit summaries
- Adverse event and protocol deviation workflows
- Continuing review and amendment preparation
- IRB submission package assembly
Key features
Plain-language consent
Consent forms drafted at an appropriate reading level with clear voluntariness, withdrawal, and contact information.
HIPAA authorization
Standalone or combined consent + authorization language depending on study design.
Pediatric pathways
Parental permission and age-appropriate assent when minors participate.
Amendment workflow
Structured process for protocol updates, consent revisions, and continuing-review timelines.
Investigator dossiers
CV, training, COI disclosures, and site capability summaries organized into a single package.
Independent review
BeaconCR does not act as the IRB. We prepare; an appropriate IRB reviews and approves.
IRB readiness is a step in a larger pathway. Once approved, the same workflows feed directly into site activation, patient registry enrollment, and HIPAA-aware data capture.
Start IRB Readiness