Compliance & Validation — Not documented by Atlas
Ask the vendor: Which compliance certifications (HIPAA, 21 CFR Part 11, SOC 2, GxP) do you hold?
Teckro
Clinical trial software making study protocols searchable for site staff, with study-wide communication tools.
Teckro, founded in 2015 and headquartered in Limerick, Ireland, digitises study protocols so site staff can search them instantly from any device, and layers study communications and oversight tools on top for sponsors. The company has raised Series C funding. It does not publish a public security certification page, so request documentation during evaluation.
- Headquarters
- Limerick, Ireland
- Founded
- 2015
- Deployment options
- cloud
- Website
- https://www.teckro.com
- https://www.linkedin.com/company/teckro
Categories
Vendor Scorecard
50% — Partial coverage. Coverage score — how completely Atlas documents Teckro across 7 buyer-evaluation areas. Reflects available Atlas data, not solution quality.
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
Mid-Size Biotech, Large Pharma, Top 20 Pharma, CRO / CDMO, Clinical Operations
Solution Scope — Documented
Natural Language Processing, Trial Protocol Optimization
Company Viability — Partially documented
Series C, Founded 2015
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
- How do sites adopt the tool in practice, and what usage rates are typical?
- How are protocol amendments propagated and confirmed with site staff?
- What security and compliance documentation can be provided?
- Which eClinical systems does it integrate with today?