Cohort paperwork. Plain text. Templates only.
We publish plain-text starting points for the four documents every cohort eventually needs: a host MSA, a participant informed consent, a CRO MSA, and an IRB / ethics submission. None of these are legal advice; have counsel review and localize before signing.
Template only - not legal advice. Each document calls out the variables to fill in{{double-braces}}; the API endpoint at /api/legal/[slug]?key=value substitutes them server-side and streams the result as a downloadable text file.
- Cohort host ↔ Peptide MD
Cohort Host Master Services Agreement
Defines the cohort host's responsibilities (pre-registration integrity, monitoring, reveal-window adherence) and the platform's role.
- Cohort host ↔ participant
Participant Informed Consent
Plain-language IC. Discloses research-use status, risks, voluntary withdrawal, leaf-hash binding, and reveal mechanics.
- CRO ↔ Cohort host (via marketplace)
CRO Master Services Agreement
Standard MSA between a CRO winning a sealed-bid auction and the cohort host. Includes data delivery and OEA reveal binding.
- Cohort host ↔ IRB / ethics committee
IRB / Ethics Submission Template
Single-document template for ethics submission. Maps the cohort's pre-registered design to the standard IRB rubric.