Risk Manager
  • Solution
    • The Validated Approval Accelerator
      • Risk Management According to ISO 14971
      • Usability Engineering According to EN 62366
      • Essential Requirements According to MDR 2017/745 & IVDR 2017/746
      • Conformity Report for Medical Electrical Equipment According to EN 60601-1
      • Risk Management for IT Networks According to IEC 80001-1
      • Process Validation According to DIN EN ISO 13485
      • Clinical Evaluation According to MDR 2017/745 & MEDDEV 2.7.1
      • Software Lifecycle Process According to IEC 62304
    • References
      • What Our Customers Say – Success Stories
      • MST-Instrumente: Work and Time Savings
      • University Hospital rechts der Isar: Faultless Documentation and Achievement of the IEC 80001-1
      • Euroimmun: Cost Savings in Usability Engineering
      • Continuous Development since 1998 – Version History
      • Selection from Our Customer List
  • Modules & Features
    • Modules
      • Risk Management
      • Usability Engineering
      • Essential Requirements
      • Medical Electrical Equipment
      • Machinery Directive
      • Requirements Engineering
      • Clinical Evaluation
      • Software Lifecycle Process
      • Medical IT Networks
      • REST API
      • Advanced Reporting
      • Pre-Validation Package
    • Features
      • Preliminary Hazard Analysis
      • Failure Mode and Effect Analysis
      • Structured Work According to Lifecycle Phase
      • Medical Device Classification
      • Post Market Surveillance
      • Self-Learning Knowledge Database
      • Fine-Grained Authorization Management
      • Visualizing with the Grey Box
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      • Individual Services
      • Medical device classification
      • Software Validation – Your Service Options
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Guide to German Medtech Companies 2021

The German medtech industry and the companies that influence it, presented on 172 pages: The sixth edition of the “Guide to German Medtech Companies 2021”, with 12,000 copies in print, has now been published internationally.

A professional framework that BAYOONET AG uses to be present with its Medical Software Division BAYOOMED as well as the Management Software Unit BAYOOSOFT.

On two pages, the guide provides an overview of the portfolio of certified experts. Specialised know-how in the development of medical software as well as advice on CE markings and FDA approvals is pushed by the BAYOOMED team. For critical infrastructures and highly regulated areas, the BAYOOSOFT Risk Manager and BAYOOSOFT Access Manager offer automated software solutions that simplify risk and authorisation management.

The BAYOOSOFT Access Manager specialises in the allocation of authorisation, administration of identities and resetting of passwords. As a fully automated software solution, the tool ensures transparent authorisation management.

BAYOOSOFT Risk Manager accelerates the approval of medical devices by generating standard-compliant technical documentation. A software solution that is the market leader worldwide. The portfolio of the business unit is rounded off by the editorially maintained, interactive reference work MediLex.

You can take a look at the “Guide to German Medtech Companies 2021” online: The guide is also available as a digital edition and mobile app.

Quelle: © BIOCOM AG

The product portfolio sounds interesting? We would be happy to provide you with more detailed information about the BAYOOSOFT Risk Manager. Just contact us.

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News

  • Mensch stapelt Holzklötze mit Symbolen aus dem Medizinbereich zu einer PyramideRisk management in the development process of medical devices: Beginning and end?8. June 2022 - 16:42
  • IVDR – End of the transition period23. May 2022 - 8:42
  • Reanimation im KrankenhausHazards and risks: This applies in risk management for medical devices10. May 2022 - 9:11
Contacts at BAYOOSOFT 

Svenja Winkler
COO/Director Management Solutions
svenja.winkler@bayoo.net

 

 

Franziska Weiß
Head of Sales franziska.weiss@bayoo.net

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