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
  • Services
    • Services
      • Individual Services
      • Medical device classification
      • Software Validation – Your Service Options
      • License Model
      • System Requirements
      • Frequently Asked Questions
    • Contact
      • Upcomming Events
      • Test Now
      • Contact Request
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A reflective Christmas season and relaxing holidays

The end of the year is approaching and with it the time for contemplative hours. We wish you a wonderful Christmas season and relaxing holidays.

We look forward to supporting you with your projects in the coming year. Until then, we wish you and your family a reflective Christmas season and a good start into the new year 2022.

In 2022, we will continue to support you with all questions and concerns regarding the preparation of technical documentation for medical devices and in vitro diagnostics.

Would you like to get to know the BAYOOSOFT Risk Manager? Then ask today for our free, 30-day TRIAL.

The BAYOOSOFT Risk Manager is your efficient way to technical documentation. In a clearly structured environment, the software solution collects all relevant information centrally, stores it in an audit-proof manner and connects it dynamically with each other in a fine-granular manner. In this way, you automatically avoid redundant data storage. Reports are generated with the most up-to-date data at the touch of a button.

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News

  • StempelBAYOOSOFT Risk Manager is DigiLab certified6. May 2022 - 9:24
  • Banner MedtecLIVEMedtecLIVE with T4M: Medical technology in focus25. April 2022 - 13:32
  • Banner MedtecLIVEMedtecLIVE with T4M: Medizintechnik im Fokus22. April 2022 - 17:04
Contacts at BAYOOSOFT 

Svenja Winkler
Product Owner & Director Management Software
svenja.winkler@bayoo.net

 

Thorsten Berndt
Product Owner
thorsten.berndt@bayoo.net

 

 

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

BAYOONET AG
Europaplatz 5
D-64293 Darmstadt

Phone: +49 (0) 6151 – 86 18 – 0
Fax: +49 (0) 6151 – 86 18 – 150

Contact: info@bayoo.net
Support: support@bayoo.net
Jobs: jobs@bayoo.net
Press: presse@bayoo.net

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Usabilty Engineering – regulatorische Anforderungen und die IEC 62366 The BAYOOSOFT Risk Manager 10.4 is now available
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