How-to articles & videos.

Practical guides to set up, run, and scale studies on ProCTTH — written by clinical operations specialists.

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Build your first study in 30 minutes

Drag-and-drop schedule of visits and form builder walkthrough.

Getting started·8 min read
Build your first study in 30 minutes

Build your first study in 30 minutes

Drag-and-drop schedule of visits and form builder walkthrough.

Setting up e-Consent the right way

Configure consent versions, signatures, and re-consent workflows.

Designing forms that subjects actually finish

UX patterns for ePRO, AE reporting, and visit forms.

Connecting wearables and IoT devices

Auto-pull vitals from smart watches into your visit forms.

ProCoins: rewarding milestones without losing blinding

Configure compensation rules tied to visit completion.

CRA mobile monitoring walkthrough

Source data verification on the go.

Setting roles: Super admin, study admin, member

Best-practice role mapping for sites and CROs.

Emergency notifications — configuration & testing

Route SAEs to the right investigator instantly.

Migrating from paper or legacy EDC

A 4-week playbook for switching mid-study.

AI-assisted protocol-to-form generation

Upload a synopsis, review the draft, publish — under an hour.

Building a decentralized cardiology trial

End-to-end DCT walkthrough with home BP cuffs and ePRO.

Site activation in under 7 days

Checklist, training plan, and the four risks to manage.

Build your first study in 30 minutes

Drag-and-drop schedule of visits and form builder walkthrough.

Emergency notifications — configuration & testing

Route SAEs to the right investigator instantly.

Setting up e-Consent the right way

Configure consent versions, signatures, and re-consent workflows.

Designing forms that subjects actually finish

UX patterns for ePRO, AE reporting, and visit forms.

Connecting wearables and IoT devices

Auto-pull vitals from smart watches into your visit forms.

ProCoins: rewarding milestones without losing blinding

Configure compensation rules tied to visit completion.

CRA mobile monitoring walkthrough

Source data verification on the go.

AI-assisted protocol-to-form generation

Upload a synopsis, review the draft, publish — under an hour.

Building a decentralized cardiology trial

End-to-end DCT walkthrough with home BP cuffs and ePRO.

Setting roles: Super admin, study admin, member

Best-practice role mapping for sites and CROs.

Migrating from paper or legacy EDC

A 4-week playbook for switching mid-study.

Site activation in under 7 days

Checklist, training plan, and the four risks to manage.