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WHPL AI Suite

AI-first products.
One regulated intelligence foundation.

Each WHPL product addresses a specific regulated workflow challenge — clinical execution, document generation, protocol creation, or evidence intelligence — built on the same governed AI platform.

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eClinical Platform
CRONOS
AI-enabled eClinical Platform

Purpose-built for BA/BE, early phase, late phase, hybrid, decentralized, and real-world clinical studies. Covers EDC, CTMS, eSource, eConsent, ePRO/eCOA, IWRS/RTSM, and AI-assisted data quality workflows.

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AI Document Generation
CronoLex
AI-Assisted CSR Generation

Generates structured, traceable, human-reviewed Clinical Study Report drafts from protocol, SAP, clinical data, PK outputs, statistical tables, and safety data — not open-ended text.

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AI Protocol Creation Platform
ProtocolGen
Structured, Review-Ready Protocol Drafts from Study Summaries

Generates structured, review-ready protocol drafts using template-governed AI, ICH M11-aligned structure, TransCelerate CPT-style content organization, curated clause libraries, and human-guided validation — for CROs, pharma, BA/BE centers, and consumer research teams.

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AI Inspection Readiness Platform
ProofOS
AI Evidence & Inspection Readiness Platform for Life Sciences

For Life Sciences QA, clinical quality, TMF, CRO, and pharma teams that need every study continuously inspection-ready — with source-linked evidence, AI-detected gaps, SOP-evidence mapping, and structured proof packs for regulatory inspection response.

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Find the right starting point.

ProductPrimary UsersProblem SolvedBest Starting Use CaseKey Outputs
CRONOSClinical Ops, CROs, Pharma, BA/BE UnitsStudy execution and clinical workflow digitizationPaperless BA/BE or hybrid study executionClinical data, workflows, dashboards, audit trails
CronoLexMedical Writing, Regulatory, CROs, PharmaCSR drafting and clinical reporting effortAI-assisted CSR draft generationCSR sections, review-ready drafts, traceability maps
ProtocolGenMedical Writers, CROs, Pharma Protocol Teams, BA/BE Centers, Consumer ResearchProtocol creation effort, inconsistency, and knowledge dependencyAI-assisted protocol drafting from study summaries with ICH M11-aligned structureProtocol drafts, clause library selections, version history, finalized protocol documents
ProofOSClinical QA, CROs, Pharma QA, TMF Teams, Sponsor OversightInspection readiness, TMF gaps, CAPA & SOP evidence fragmentationContinuous inspection readiness & TMF QC intelligenceInspection proof packs, gap reports, TMF completeness maps, SOP-evidence matrices

Not sure which product fits your workflow?

Share your challenge and WHPL will identify the most relevant product, demo, or pilot approach for your team.