Security · Privacy · Life Sciences — one platform
Everything you're audited on. In one place.
Prepare for audits with shared controls, evidence, and clear ownership across security, privacy, and life sciences — for your team or every client you manage.
Service status and incident updatesFree Community plan · one framework · up to two users · Compare plans
Show me what fits — I work in
Turn audit requirements into a clear work plan.
Connect controls, supporting evidence, and the people responsible for the next step.
- Map a control across frameworks
- Attach the supporting evidence
- Assign the remaining work
Information Security Policy
ISO 27001 A.5.1 → NIST CSF
- Evidence
- Policy document · awaiting review
- Next action
- Review evidence for the next audit
Security & IT
Controls, risk, audits, vendors
- Control library· 1,400+
- Risk tracking & indicators
- Internal audits & CAPA
- Vendor risk & access reviews
Privacy
Consent, DSRs, data mapping
- Cookie consent & scanning
- Data requests & deadlines
- Processing records & data flows
- Privacy by Design gates
Life SciencesQuality & regulation
GxP / GMP for pharma & biotech
- Corrective actions & root cause
- Supplier qualification
- System validation & traceability
- Part 11 e-signatures
One platform instead of a security tool + a privacy tool + a QMS + spreadsheets.
01 / Efficiency
One control library, mapped across frameworks.
Frameworks overlap heavily. CompliOne records how each control maps to the other frameworks it supports — with the match type and strength — so you implement once and reuse the evidence instead of starting each audit from scratch.
Information Security Policy
From the reviewed mapping library
- ISO 27001A.5.1source
- SOC 2CC1.1partial · 70%
- NIST CSFGV.RM-05related +4
- FEDRAMPAC-1related +8
Batch Record BR-2291
Approved for release
- Signed by
- A. Levi · QA Manager
- Meaning
- Approval
- Timestamp
- 2026-07-14 09:22 UTC
- Hash chain
- 9f2a…c41
Immutable audit trail — each entry hash-chained to the last.
02 / Life Sciences
The regulations most GRC platforms don't touch.
CAPA, supplier qualification, computer-system validation, and 21 CFR Part 11 signatures — alongside ISO 27001 and GDPR, on one evidence store. Pharma and biotech stop stitching a QMS to a GRC tool.
03 / AI Copilot
AI does the grunt-work.
An agent that maps controls across frameworks, flags gaps in real time, and generates policies from your templates — grounded in your real evidence, not guesswork.
// analyzing your controls against SOC 2…
→ found 3 gaps — CC6.1, CC7.2, CC8.1
Draft the fixes and map them across your frameworks?
Acme Biotech
ISO 13485 · ISO 27001
94%Vertex Health
GDPR · SOC 2
89%Kestrel Fintech
PCI-DSS · SOC 2
82%
Many clients · one login · under your brand
04 / For Agencies
Run it for every client.
Manage multiple clients, build per-client workplans and budgets, generate board reports, and white-label the platform as your own.
Learn moreThe consolidation
Replace the stack you're stitching together.
- Replaced:
- a security tool
- a privacy tool
- a QMS
- Excel trackers
- a client portal
- shared drives
Privacy in practice
Beyond the headline: workflows, decisions and evidence
Map data, work requests, review suppliers and prepare privacy notices—with visible review status and no automatic compliance promise.
Explore privacy solutionsData inventory
Systems, categories, purposes and owners
Suppliers
Documents, evidence and review decisions
Rights
Requests, identity checks and responses
Israel
Privacy records and notice drafts
See your whole compliance picture in one place.
One platform for security, privacy, and life sciences.
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