Field Guide

Operational knowledge for the parts of clinical data and analysis delivery that functional manuals do not teach.

Twenty-one practitioner-oriented guides focused on decisions, failure modes, handoffs, evidence, and delivery readiness from startup through regulatory submission.

How to use this

Read for the reasoning, not just the checklist.

Each guide explains the decision points and failure modes behind a checkpoint, not just what to check.

01

Start with the situation

Search for the operational problem you are facing, not only a standard name.

02

Identify the decision and failure mode

Use the guide to distinguish function-specific work from upstream data, statistical, clinical, regulatory, or governance decisions.

03

Translate guidance into action

Open Navigator when you need dates, ownership, collaborators, and closure evidence around a real milestone.

Standards and regulatory context

Use practice guidance alongside current authoritative requirements.

The Field Guide deliberately focuses on operational execution across clinical data and analysis delivery. For submission standards, metadata, electronic submission, GCP, and statistical principles, use the official reference library and confirm the version applicable to the program and region.

Open industry reference library

Common reference families

  • FDA study-data and eCTD technical guidance
  • CDISC SDTM, ADaM, implementation guides, and conformance rules
  • ICH E6(R3), E9/E9(R1), and CTD/eCTD materials
  • Sponsor procedures, controlled terminology, and submission-specific instructions