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Choose your pricing plan

Per Process Desciption, Standard Operating Procedure (SOP), or Work Instruction (WI)

  • Digital QMS Transformation

    3,200CHF
    Every month
    +CHF 38,400 12 Initial Digital Transformations
    12 Customized Process Descriptions
    Valid for 12 months
    • Live, Content-Rich Process Descriptions
    • Atomic Traceability
    • 300 Content-Rich Technical Templates
    • Comprehensive Medical Device Regulatory Requirements Package
    • 10 Standard User Licenses (ISO & IEC) for 1 Site (Cost incl.
  • Best Value

    Pilot Department QMS Compliance

    3,600CHF
    Every month
    +CHF 38,400 12 Initial Digital Transformations
    12 Continuously Upgraded Process Descriptions
    Valid for 12 months
    • All Prior Features Plus These Exclusive Benefits:
    • Stay Compliant: Regulatory Change Impact Assessment Incl.
    • Unlimited Standard User Licences for 5 Sites (Cost incl.)
    • Expandable Medical Device Regulatory Database
  • Multi-Site-Department QMS Compliance

    0CHF
     
    Price upon Request
    Free Plan
    • 24h Premium Support
    • Any additional data package (e.g. standard, guideline)
    • Multi-Language Processes with AI Translation Capability
    • API to Document Management System
    • API to Requirement Engineering Tool
    • Certification Package for ISO 13485
    • Certification Package Cyber Security for ISO 27000
    • Digital Signature and Computer System Validation Package for
  • Start-Up QMS Compliance

    1,800CHF
    Every month
    +CHF 3,200 Tailoring to your needs
    12 Ready-to-Use Process Descriptions
    Valid for 12 months
    • Live, Content-Rich Process Descriptions &Atomic Traceability
    • Atomic Traceability
    • Comprehensive Medical Device Regulatory Requirements Package
    • 3 Standard User Licenses (ISO & IEC) for 1 Site (Cost incl.)
    • 12 Process Description Minimum Purchase (Per-SOP Pricing)
  • Medical Device Product Compliance

    17,790CHF
    Every year
    e.g. IEC 60601-1 Series Data Package
     
    • Online Product Requirement Interpretation Functionality
    • Ready for Interpretation: IEC / ISO in Clause Resolution
    • Systematic & Atomic Traceability to Product Requirement
    • 10 IEC Standard Users Licences for 1 Site (Cost incl.)
    • Expandable with any ISO, IEC or other Regulatory Data
    • Compliance Reporting per Standard or Regulation

ADD-ONs

Integrate ColabON into Your Compliance Infrastructure

  • Any additional data package (e.g. regulation, standard, guideline) 

  • Interface to Document Management System

  • Interface to Requirement Engineering Tool

  • Certification Package for ISO 13485

  • Certification Package Cyber Security for ISO 27000

  • Digital Signature and Computer System Validation Package for ISO 13485

  • Multi-Language Processes with AI Translation Capability

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Features

01.

Access the latest regulatory information, officially licensed and promptly accessible online.

02.

Live QMS with Version-controlled Process Elements  

03.

Atomic Traceability: the ability to trace every element of a process or product back to its original regulatory requirement.

04.

Impact Analysis: Identify regulatory changes early and assess their impact quickly.

05.

REAL-TIME QMS Reporting and  Dashboard

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