The AI-native marketplace for B2B

Marketplace

  • Marketplace home
  • Search
  • Products
  • Services
  • Companies

Developers

  • Docs
  • MCP server
  • Public API
  • API reference
  • Versioning

Agents

  • Claude Code
  • Claude Desktop
  • Codex
  • Cursor
  • VS Code Copilot
  • ChatGPT

Legal

  • Privacy Policy
  • Terms of Service
  • Cookie Policy
  • Data Processing Agreement
  • Subprocessors
  • Report content
Tradebird agent

Tradebird

What does your business need?

  1. Marketplace
  2. /Services
  3. /Automation & digital services
  4. /Robot & production-line integration
  5. /Assembly automation integration
  6. /
  7. Medical production automation
Assembly automation integration

Medical production automation

Kilde A/S AutomationUlvevej 21, 7800 Skive, Denmark

Assembly, process and packaging automation designed around customer documentation, traceability and cleanroom requirements.

Automation qualification documentation
Requirements traceability; functional, hardware and software design specifications; design reviews; IQ/OQ protocols and version-controlled documentation for supplied automation.
Validation route
GMP-based project validation connects URS, risk analysis, design and testing with FAT, SAT and subsequent IQ/OQ.
Price

Price on request

View on supplier website
Kilde diagram of scalable medical automation stagesSource: kildeautomation.com

Ask Tradebird

Private to you. Nothing is shared with Kilde A/S Automation automatically.

KA
Kilde A/S Automation
Ulvevej 21, 7800 Skive, DenmarkKilde develops and builds custom automated production equipment in Skive. Its work combines mechanical, electrical and software engineering with assembly, process integration, packing and palletising. It also supplies modular packaging and medical automation families and supports installed equipment through maintenance, repair and spare parts. Founded in 1970, Kilde has operated within the BILA Group since April 2022. The Kilde Archive System, also marketed as Slide Manager at Axlab, integrates with laboratory information systems (LIS) to register, store and retrieve tissue slides. Its modular design can support other traceable storage applications.
View company

About this service

Assembly, process and packaging automation designed around customer documentation, traceability and cleanroom requirements. Requirements traceability, functional and hardware/software design specifications, design reviews, IQ/OQ protocols and version-controlled documentation for supplied automation. GMP-based validation connects URS and risk analysis with design, testing, FAT, SAT and subsequent IQ/OQ.

Service details

Automation qualification documentation
Requirements traceability; functional, hardware and software design specifications; design reviews; IQ/OQ protocols and version-controlled documentation for supplied automation.
Validation route
GMP-based project validation connects URS, risk analysis, design and testing with FAT, SAT and subsequent IQ/OQ.