Docs home
Start from the canonical documentation home, standards, and reference map before diving into individual features.
Start hereDocumentation for Chokmi — Africa's clinical trial activation and evidence intelligence OS. Country setup, multilingual consent, patient matching, protocol compliance, and inspection-ready evidence.
Choose the guide that matches your role — country activation, evidence operations, AI review, or platform administration.
Start from the canonical documentation home, standards, and reference map before diving into individual features.
Start hereCanonical workflow for editing, optimization, pretest, and conversation preview across study instruments.
Learn workflowsEnd-to-end guide for channels, quotas, site activation, panel connectors, and trial automations.
Explore featuresCanonical guide for live monitor, audit history, AI review, reviewer consensus, and quality settings.
See examplesCanonical troubleshooting and support runbook entrypoint for all major product areas — covers activation, consent, matching, and evidence flows.
Get helpComplete workflow for file upload, mapping, preview, and final import into the operating record.
Open guide33 custom functions, progressive AI learning, rich entity data types, streaming cells, and the full 10-tab Research Studio inside Excel.
Excel feature guide30 custom functions, reactive onEdit coding, one-click install, centralised codebook with dropdown, and the research pipeline macro.
Sheets feature guideChoose the right spreadsheet path: Excel, Google Sheets, Numbers, LibreOffice, or the browser bridge fallback.
Browse guidesDifferent paths for different goals — find the one that fits your role on the trial.
Start with Docs home (15 min) → Open your first study and country track → Return to Survey & protocol authoring when you need deeper knowledge.
Use the quick reference in Docs home to find exactly where to go, then jump to that section in Feature guides.
Check Troubleshooting first. Still stuck? Email tech@chokmi.com or use in-app chat for help.
Share Docs home with everyone. Then assign role-specific reading: sponsors → outcomes, CRO leads → core workflows, sites → activation & consent, regulatory → evidence intelligence.
Understand these core ideas before diving into the guides — they map directly onto how Chokmi structures activation and evidence.
A live readiness score for each study, country, site, and evidence package — checks completeness, protocol compliance, missing documents, and review coverage.
Every claim links back to source documents, consent records, protocol criteria, patient facts, reviewer actions, and model outputs.
Multilingual consent, comprehension checks, translation review, and signature provenance tied to the protocol version that was active.
Checks whether actions follow the approved methodology, protocol version, regulatory requirements, and review thresholds.
See where reviewers agree, where AI disagrees with humans, and where senior review is needed before decisions are final.
Important assertions can be stress-tested, signed, and exported with their supporting and contradicting evidence.
10 coding methods (thematic, in-vivo, descriptive, etc.) with AI-assisted code suggestion, inter-rater reliability, and codebook management.
Every coding decision, weighting correction, and analysis step is logged with transparent methodology — defensible by default.
Follow this six-step path to take a study from country setup to inspection-ready evidence.
Understand what Chokmi does, learn the operating record concept, and see the complete first-study walkthrough. About 15 minutes.
Open a study, switch on the countries you need, and bind country rulepacks to your activation tasks, requirements, and submission packages.
Configure multilingual consent flows and bias-aware patient matching. Every translation, review, and match decision lands in the operating record.
Sponsor, CRO, and site teams work inside the same record. Tasks, dependencies, and evidence stay connected instead of fragmented across trackers.
Use the Trial Passport, evidence completeness scoring, reviewer consensus, and bias diagnostics to find issues before they become inspection findings.
Generate inspection-ready exports backed by the Evidence Graph, Claim Passport, and Ed25519-signed evidence capsules.
At a glance: what's in each guide, who it's for, and how long it takes to read.
| Guide | What's inside | Best for | Reading time |
|---|---|---|---|
| Docs home | Platform overview, core concepts, first-study walkthrough, quick reference | Everyone new to Chokmi | 15 minutes |
| Core workflows | Activation, consent, matching, qualitative coding, distribution, analysis, reporting, team management | Researchers and CRO operators | 50 minutes |
| Feature guides | Deep dives: survey builder, qualitative coding, distribution, data studio, weighting, quality monitoring, methodology as code, consultation analysis, permissions, integrations | Power users and admins | 60 minutes |
| Real-world scenarios | Worked examples: sponsor multi-country oversight, CRO delivery coordination, ethics review handoff, regulatory inspection | Anyone wanting practical applications | 40 minutes |
| Troubleshooting | Common problems, solutions, error messages, frequently asked questions | Anyone stuck on a specific issue | As needed |
Show us where country setup, eligibility, consent, patient matching, or evidence review is breaking. We will show you how Chokmi structures it into an activation and evidence intelligence workflow.