Viedoc

eClinical suite (EDC, RTSM, eCOA, eTMF) from Sweden with an audited ISO 27001 certificate and documented 21 CFR Part 11 compliance.

Viedoc Technologies, founded in 2003 and headquartered in Uppsala, Sweden, provides an eClinical suite spanning EDC, RTSM, eCOA/ePRO, and eTMF used in global trials. It publishes an audited ISO 27001 certificate on its own site and documents 21 CFR Part 11 compliance for the platform (a conformance claim rather than a certification). Validate the depth of any AI-assisted features versus core data-capture workflows during evaluation.

Headquarters
Uppsala, Sweden
Founded
2003
Compliance
ISO 27001, 21 CFR Part 11
Deployment options
cloud
Website
https://www.viedoc.com
LinkedIn
https://www.linkedin.com/company/viedoctechnologies

Categories

AI Use Cases

  • Clinical Data Management

Vendor Scorecard

64% — Partial coverage. Coverage score — how completely Atlas documents Viedoc across 7 buyer-evaluation areas. Reflects available Atlas data, not solution quality.

Compliance & Validation — Documented

ISO 27001, 21 CFR Part 11

Deployment & Hosting — Documented

cloud

Pricing Transparency — Not documented by Atlas

Ask the vendor: What is your pricing model, and what drives total cost of ownership?

Implementation & Onboarding — Not documented by Atlas

Ask the vendor: What is a realistic implementation timeline, and what onboarding support is included?

Organization & Role Fit — Documented

Biotech Startup, Mid-Size Biotech, Large Pharma, CRO / CDMO, Clinical Operations, Data Management

Solution Scope — Documented

Clinical Data Management

Company Viability — Partially documented

Private, Founded 2003

Always ask the vendor

Not captured in Atlas data — confirm directly. Excluded from the score above.

Data Rights & IP

Who owns model outputs? Is our proprietary data used to train models others can access, and where does our data reside?

Model Credibility & Explainability

Can you share validation studies or benchmarks, explain how the model reaches its conclusions, and describe how bias and drift are monitored?

Questions to Ask This Vendor

  • Which modules (EDC, RTSM, eCOA, eTMF) are most mature for our trial design?
  • What AI-assisted capabilities exist today versus roadmap?
  • How is Part 11 compliance evidenced beyond the vendor's own claim?
  • What regulatory-inspection track record exists in our target regions?