Acodis

Intelligent document processing platform digitising manufacturing and quality documents such as batch records.

Acodis, founded in 2016 and headquartered in Winterthur, Switzerland, provides an intelligent document processing (IDP) platform that extracts structured data from complex documents, with a focus on pharmaceutical manufacturing and quality documentation. Data is hosted in Switzerland, and the company has raised Series A funding. It does not publish security certifications, so request documentation — including any GMP-relevant validation support — during evaluation.

Headquarters
Winterthur, Switzerland
Founded
2016
Deployment options
cloud
Website
https://www.acodis.io
LinkedIn
https://www.linkedin.com/company/acodis-i-o

Categories

AI Use Cases

  • Manufacturing Quality Control

Vendor Scorecard

50% — Partial coverage. Coverage score — how completely Atlas documents Acodis across 7 buyer-evaluation areas. Reflects available Atlas data, not solution quality.

Compliance & Validation — Not documented by Atlas

Ask the vendor: Which compliance certifications (HIPAA, 21 CFR Part 11, SOC 2, GxP) do you hold?

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, IT / Digital, Data Management

Solution Scope — Documented

Natural Language Processing

Company Viability — Partially documented

Series A, Founded 2016

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

  • What validation support is available for GMP-regulated document workflows?
  • What security and compliance documentation can be provided?
  • Which document types and languages does the extraction handle well today?
  • Can data be hosted in regions other than Switzerland if required?