A protocol that locks the method before the results are seen.

Protocol plus the IRB submission. Fixed fee, defined deliverable, reproducible code.

Sample protocol contents and ethics submission checklist

Protocol & ethics submission package

What you get, and how it runs.

The full study protocol, objectives, design, population, exposures and outcomes, covariates, pre-specified statistical analysis plan, and sample-size justification, written to the reporting standard your design will be judged by (STROBE, RECORD, PRISMA-P, TRIPOD, or SPIRIT), plus the complete package your ethics committee or IRB expects.

How it works

  1. We agree the question, data source, and the outcomes that matter to you.
  2. We draft the protocol with a pre-specified analysis plan and table shells.
  3. We prepare the ethics / IRB forms, consent materials where required, and the data-handling statement.
  4. For systematic reviews we register the protocol on PROSPERO.

What you get

  • Full protocol with pre-specified statistical analysis plan
  • Table shells and figure list
  • Ethics / IRB submission package and consent materials
  • PROSPERO registration for evidence syntheses
  • Reporting-guideline checklist mapped to the protocol

$900 per project · typically 1 to 2 weeks

Request a protocol

How single-task work runs

Four steps from enquiry to delivery.

01

Send what you have

Dataset, draft, idea, or rejection letter

02

Scope

What the stage needs, within two working days

03

Fixed quote

Scope, timeline, fee in writing

04

Delivery

Deliverable, code, handover note

Test the fit at no cost

Send your area of interest, one idea, or one stalled dataset.

You get a short feasibility note, design, expected sample, realistic journals, free of charge.