healthcare

Clinical workflow automation for hospitals and research organizations

Governed clinical operations. From protocol to patient record.

Person holding and reviewing multiple printed documents at a desk with a monitor and tablet displaying colorful charts.
Trusted by +10,000 customers
The challenge

Clinical precision ends where the process becomes manual.

A clinical protocol is defined. It is documented in a PDF. Teams follow it, mostly. Exceptions are handled informally. When an FDA inspector asks for evidence of protocol adherence on a specific date, the answer lives in someone's email archive.

Protocol adherence that depends on individuals

Clinical protocols exist in documents, not enforced processes. Adherence depends on individuals following guidelines, creating variation, risk, and compliance exposure.

Data entry errors in high-stakes environments

Manual data collection in lab and clinical settings introduces errors that compound through the research or care process, affecting outcomes, invalidating results, and triggering regulatory scrutiny.

Regulatory reporting that consumes clinical time

FDA, EMA, and hospital accreditation requirements demand documented evidence of every clinical action. Assembling that evidence manually takes time clinical teams don't have.

A man and a woman working together at a laptop in a warm-toned office with a wooden wall background.
Bonita solution

From clinical protocol to compliant execution. In Bonita.

Bonita models clinical protocols and lab workflows as governed process applications — from patient enrollment and sample collection through data recording, result validation, and regulatory reporting. Every step enforces the protocol. Deviations trigger escalation automatically. Lab systems, EHRs, and data platforms integrate without manual transfer. Every clinical action generates a compliance record that meets FDA, EMA, and hospital accreditation standards, without clinical staff spending time on documentation.

Protocol enforced as process

Clinical steps are not guidelines — they are enforced workflow gates. Every action follows the protocol. Every deviation is flagged automatically.

Automated data capture

Lab results, sample tracking, and clinical observations feed into the process automatically, reducing errors and freeing clinical staff from manual recording.

Regulatory records generated in real time

Every clinical action logged with full context as it happens. FDA, EMA, and accreditation records are current and complete — not assembled retrospectively.

Full exception traceability

Every protocol deviation logged, escalated, and resolved through a governed path. No undocumented exceptions, no compliance gaps.

Meet the challenge with Bonita process automation

The capabilities that make clinical operations precise, governed, and compliance-ready at every protocol step.

1

BPMN 2.0 process modeling

Model clinical protocols and trial workflows visually, including deviation paths, escalation rules, and approval chains, with full exception handling built in before deployment.

2

Business rules engine

Encode protocol requirements, regulatory thresholds, and decision criteria per trial phase. Every step enforces the protocol, no deviation passes without triggering the defined escalation path.

3

Lab and EHR integration connectors

Connect lab information systems, electronic health records, and clinical data platforms into a unified workflow. Data flows without manual transfer, eliminating errors at source.

4

Intelligent Document Processing

Extract and classify data from clinical forms, lab reports, and regulatory submissions automatically before injection into governed workflow steps.

4

Full audit trail

Every protocol step, clinical action, and deviation logged with timestamp and full context. FDA, EMA, and hospital accreditation records generated in real time, not assembled retrospectively.

6

AI connectors (OpenAI / Mistral)

Analyze clinical data, flag anomalies in assay results, and generate structured summaries within fully auditable execution paths, AI enriches, the engine enforces.

Main KPIs

5 FTE
equivalent time savings through process automation
500+
assay requests processed daily with reduced errors
Data
errors reduced and accuracy improved across drug discovery workflows
A man and a woman working together at a laptop in a warm-toned office with a wooden wall background.

"Digitizing our paper-based analytical process has resulted in time savings equivalent to 5 FTEs. Our scientists are now focused on data interpretations rather than performing manual tasks."

Head of operations

Bristol Myers Squibb

Related use cases

Care management

Discover care management using Bonita

Link to

Compliance automation

Discover compliance automation using Bonita

Link to

Financial Accounting

Discover financial accounting using Bonita

Link to
Frequently asked questions
How does Bonita support clinical trial compliance?
Bonita models trial protocols as enforced process workflows, every step is a governed gate, not a guideline. Deviations trigger escalation automatically. Every action generates a compliance record that meets FDA, EMA, and ICH standards without manual documentation effort.
Can Bonita integrate with lab information systems and EHRs?
Yes. Bonita connects to LIS, EHR, and data management platforms through its connector library and open APIs. Lab results, patient records, and sample tracking data flow into clinical workflows without manual transfer, eliminating errors at the data entry point.
How does process automation reduce the documentation burden on clinical staff?
Clinical actions are logged automatically as they happen — no separate documentation step required. Regulatory records are generated in real time, not assembled retrospectively. Clinical staff focus on protocol execution, not recordkeeping.

Work that scales with your enterprise

Recognition and projection of how work evolves across your organization