IRB Consent · In Development
Informed consent,
done right.
Full IRB consent framework is in production.

We're building a comprehensive informed consent system under IRB Protocol PPRN-001-2025 — covering clinician enrollment, patient consent workflows, adverse event reporting, and outcomes data capture. In the meantime, IRB forms and enrollment are available through your Peptide Pure clinician account.

Framework

IRB Protocol PPRN-001-2025

Full informed consent framework for the Practice-Based Patient Registry Network. Covers clinician responsibilities, patient enrollment criteria, and data governance standards.

Clinician

Provider Enrollment & Credentialing

NPI verification, IRB consent at login, certification tracking, and clinic-level compliance documentation. Automatic enrollment through your Peptide Pure account.

Patient

Patient Consent Workflows

Digital informed consent forms, treatment authorization, risk disclosure templates, and patient-facing education materials for regenerative medicine protocols.

Safety

Adverse Event Reporting

AE/SAE report templates, severity grading, causality assessment, and escalation pathways. Structured data capture for safety monitoring and outcomes tracking.

Data

Outcomes & Compliance

Patient outcomes data capture, treatment log templates, baseline assessments, and building a defensible compliance structure for your practice.

Clinical Forms → Enroll at Peptide Pure → FAQ →