Features Built for Secure Document Exchange

Every capability designed to meet the security, compliance, and oversight requirements of regulated industries.

Purpose-Built for Life Sciences

DataRoomr addresses the unique requirements of pharma and biotech transactions.

Pharmaceutical Due Diligence

Share pre-clinical data, regulatory filings, and IP documentation with potential acquirers. Watermarked viewing prevents unauthorised distribution of proprietary research.

Life Sciences M&A

Manage complex multi-party transactions with granular access controls. Assign different document visibility to each bidder group while maintaining complete audit oversight.

Clinical Trial Data Sharing

Share clinical trial results and regulatory submissions with partners and investors. Page-level tracking shows exactly which documents received attention and for how long.

Comprehensive Feature Set

Secure Document Viewer

Documents render on a secure canvas — never as downloadable files. Dynamic watermarks overlay every page with the viewer's identity, deterring unauthorised screenshots and distribution.

  • Canvas-based rendering (no PDF downloads)
  • Dynamic watermarks with viewer identity
  • Screenshot deterrent technology
dataroomr.io/room/acme-pharma/view j.smith@investor.com j.smith@investor.com Secure View Protected Downloads Blocked Page 3 of 24
Access Controls + Add Group A Alpha Bidder Group 4 investors · Full access Active Edit B Beta Bidder Group 2 investors · Limited access Active Edit L Legal Advisors 3 investors · Regulatory docs only Pending Edit NDA required before access

Granular Access Controls

Control document visibility at the folder and individual document level. Group investors with shared permissions, or set per-investor overrides for sensitive materials.

  • Folder and document-level permissions
  • Investor group management
  • NDA enforcement with version tracking

Immutable Audit Trail

Every action is logged permanently. Track page-level viewing activity, document access, and user sessions with exportable reports for regulatory compliance.

  • Page-level view tracking with time spent
  • Immutable event logging
  • Exportable compliance reports
Audit Trail Export CSV Jane Smith viewed Clinical-Phase2-Results.pdf Pages 1–8 · 14 min 32s · IP: 82.132.xxx.xxx 2 min ago Mark Chen signed NDA v2.1 Digital signature recorded · NDA-2024-0847 18 min ago Sarah Lee attempted screenshot (blocked) IP-Portfolio-Summary.pdf · Page 3 · Watermark triggered 1 hr ago Admin uploaded Regulatory-Filing-Q3.pdf 24 pages · v1.0 · Folder: Regulatory Submissions 3 hrs ago
Documents 1. Financial 1.1 Revenue Model.pdf 1.2 Projections.pdf 1.3 Cap Table.xlsx 2. Regulatory 3. IP Portfolio 4. Clinical Data 1.2 Projections.pdf v3.0 (current) Uploaded 2 days ago Latest v2.0 Uploaded 2 weeks ago v1.0 Uploaded 1 month ago 24 Pages 18 Views 4.2m Avg. Time Upload New Version

Document Management

Organise documents with folder hierarchies and reusable templates. Version control maintains a complete history while presenting only the latest version to investors.

  • Version control with full history
  • Reusable folder templates
  • Section numbering and ordering

Q&A Workflow

Investors submit questions tied to specific documents or pages. Route questions to the right team members and track response times across the entire due diligence process.

  • Document-linked questions
  • Team routing and assignment
  • Exportable Q&A reports
Q&A — Acme Pharma Room 12 Open 34 Closed Can you clarify the Phase 2 endpoint criteria? Re: Clinical-Phase2-Results.pdf, Page 12 From: Jane Smith (Alpha Group) · 3 hrs ago Pending DR Assigned What is the patent expiry timeline for Compound X? Re: IP-Portfolio-Summary.pdf, Page 5 From: Mark Chen (Beta Group) · 1 day ago Answered Are there any ongoing FDA correspondence re: warnings? Re: Regulatory-Filing-Q3.pdf, Page 1 From: Sarah Lee (Legal Advisors) · 2 days ago Urgent
phase 2 clinical endpoints Search 7 results found across 3 documents PDF Clinical-Phase2-Results.pdf ...primary endpoints demonstrated in Phase 2 clinical trials... Page 8, 12, 15 PDF Regulatory-Filing-Q3.pdf ...Phase 2 safety profile and endpoint definitions per FDA guidance... Page 3, 7 XLSX Trial-Data-Summary.xlsx ...clinical endpoint comparison table for Phase 2 cohorts A-D... Sheet 2 Access OK

Full-Text Search

Search across all documents within a data room. Results respect access permissions — investors only see documents they are authorised to view.

  • Search within document content
  • Permission-aware results
  • Filename and content matching

Security & Data Residency

Your documents are protected at every layer — from encryption at rest to region-locked storage that keeps data where your regulations require.

Choose Where Your Data Lives

UK-headquartered and subject to UK data protection law, DataRoomr lets you select a data residency region per data room. Documents are stored in the region you choose and never leave it — ensuring compliance with GDPR, PDPA, data sovereignty laws, and internal governance policies.

🇺🇸 United States

US East (Virginia)

🇪🇺 Europe

London, UK

🇸🇬 Asia-Pacific

Singapore

Data Residency Room Settings US East London Singapore Select region for this room: US East Virginia, US Europe London, UK Asia-Pacific Singapore

Encryption Everywhere

AES-256 encryption at rest on all stored documents. TLS 1.2+ in transit. Your files are encrypted before they reach the disk and stay encrypted until authorised viewing.

All Plans

Tenant Isolation

Every organisation's data is fully isolated on every plan. AES-256 encrypted storage, tenant-scoped access controls, and strict boundaries at the database, storage, and application layers keep your data separate by default.

Pro & Enterprise

Dedicated Storage Boundary

Go further with a dedicated AWS storage access point scoped exclusively to your organisation. An infrastructure-level policy physically prevents cross-tenant access — verifiable and auditable by your security team.

Compliance Ready

Architecture aligned with 21 CFR Part 11, HIPAA, and GDPR requirements. Immutable audit logs, access controls, and data residency give your compliance team the evidence they need.

Beyond Pharma

While built with pharmaceutical and life sciences transactions in mind, DataRoomr serves any industry requiring secure document exchange — legal due diligence, financial M&A, real estate transactions, and fund management.

See How DataRoomr Works for You

Start your 14-day free trial or explore our pricing options.