Life Sciences
Woork for Life Sciences runs clinical trial operations, HCP engagement, regulatory tracking, and quality events on one low-code platform, the functional depth of enterprise clinical-trial software, configurable by your own team instead of a six-figure validation engagement.
Clinical Trial Management
Study and site tracking with per-site activation status, principal investigator assignment, and country-level rollout, so slippage is visible the moment it happens, not at the next steering committee.
Per-site activation status, PI assignment, and country-level rollout visibility.
Planned-vs-actual dates, so slippage shows up immediately.
Site initiation, interim, and close-out visits, with findings logged against the visit.
Payment tracking tied directly to visit and enrollment milestones.
Enrollment
Planned, forecast, and actual counts at every stage, consented, screened, enrolled, randomized, withdrawn. Pure aggregate metrics, zero patient-level data, by design.
Planned, forecast, and actual at every funnel stage.
See where recruitment is tracking ahead or behind, per site.
Counts only, no patient-level records ever enter the system.
Roll enrollment up by site, country, or the whole study.
eTMF & Site Activation
Site activation checklists built against the industry-standard TMF Reference Model document zones, no guessing what's required, and per-site document status a coordinator can read at a glance.
Activation checklists mapped to the standard document zones.
Completion status per site, so nothing outstanding is a surprise.
See exactly what's left before a site can start enrolling.
The outstanding-items list, from the coordinator's seat.
HCP Engagement & Compliance
Field call reporting in seconds, account, call type, products discussed, and a sample-disbursement gate a rep cannot get past. A call can't be submitted with a sample quantity over the license limit, full stop.
Account, call type, and products discussed, logged in seconds.
Submission blocks when a sample quantity exceeds the license-defined limit.
Aggregate spend across calls and samples, ready for reporting.
Track which products were detailed, by account and by rep.
AI Agents
Bounded jobs across trial ops, regulatory, and compliance, with hard gates where a rule can't be crossed.
Chases outstanding eTMF checklist items per site and nudges the responsible owner before activation stalls.
Turns visit notes into structured follow-up items automatically, so nothing from a site visit gets lost.
Watches Health Authority question due dates and flags anything approaching or past deadline.
Drafts the call report from field notes and blocks submission if sample quantities exceed license limits, before it becomes a finding.
Regulatory & Quality
Applications through Health Authority review, with a running log of questions and response due dates so nothing slips.
Root-cause tracking with a defined path to CAPA, corrective and preventive actions tracked separately, each with an owner and due date.
A full approval lifecycle: pending approval, in approval, approved, implementation, closed.
Why Woork for Life Sciences
CTMS, eTMF, HCP engagement, regulatory tracking, and quality management, without the validation-project price tag.
Your own team adds a field or changes a workflow, no consulting engagement required.
Trial ops, regulatory, and quality in one place instead of a stitched-together set of point solutions.
Built for the mid-market and CRO teams the enterprise players price out.
Talk to us
Tell us what you're building. We'll show you Woork on your own use case, apps, agents, and integrations, governed by default.
Not a canned demo. We'll stand up your use case on the platform so you can see the real thing.
You'll speak with someone who can actually architect it, forward-deployed, hands on the keys.
See how fast a governed, enterprise-grade app ships, days, not months.
Prefer email? hello@dowoork.com