Product Portfolio

Industry-specific solutions built on the Cohera platform. Each product is designed for the unique compliance challenges of regulated industries.

BioWise

Live

Pharmaceutical Compliance Platform

Purpose-built for pharmaceutical quality management, supplier oversight, and regulatory documentation. BioWise connects your legacy systems and automates compliance workflows.

Industries

Pharmaceutical Biotech CDMO

Compliance

21 CFR Part 11 EU GMP Annex 11 ICH Q10
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Key Capabilities

  • Certificate of Analysis management
  • Supplier qualification workflows
  • Change control automation
  • Expiry and renewal tracking
  • Audit trail and e-signatures
  • AI-powered document intake

MediWise

Coming 2026

Medical Device Compliance Platform

Designed for medical device manufacturers to manage design controls, risk management, and post-market surveillance with full regulatory traceability.

Industries

Medical Devices IVD Combination Products

Compliance

21 CFR Part 820 EU MDR 2017/745 ISO 13485
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Key Capabilities

  • Design History File (DHF) management
  • Risk management per ISO 14971
  • CAPA and complaint handling
  • Post-market surveillance
  • UDI compliance tracking
  • Supplier quality management

Coming Soon

We're expanding the Cohera platform to serve more regulated industries.

LabWise

2027

Laboratory information management for regulated environments.

ClinWise

2027

Clinical trial document management and TMF compliance.

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Our team will walk you through the capabilities most relevant to your organization.

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