risk-analysis, DIN 14971, risk-management, medical-devices
Risko analysis, DIN 14971, Risk management Medical devices, In-Vitro-Diagnostics, IVD DEUTSCH | IMPRINT 19.05.2012 FDA notification, CE-marking, EN 1441 Qware Riskmanager
risk-analysis, DIN 14971, risk-management, medical-devices
seminars software market analysis accomodation certification notified body product lifecyclerisk management report Risk analysis of medical devices DIN EN ISO 14971
admission of medical products implementation of risk management for medical devices harmonized norm
ISO 9000 implementing of a Risk analysis risk control
post production information implementation of risk management according to DIN EN 14971
post production information implementation of risk management according to DIN EN 14971
risk management versus Risk analysis documentation
seminars post production information risk management report
DIN EN ISO 14971 In-Vitro-Diagnostics CE-marking
FDA authorization CE-marking
Qware Riskmanager
product lifecycleRisk analysis of medical devices post production information
harmonized norm DIN EN 14971
accomodation certification notified body
 implementation of a risk analysis risk management normative law regulations
Likelihood and severity evaluation after measures
DIN EN ISO 14971:2000
assignment with DIN EN ISO 13485_2003
product process severity measures evaluation likelihood
life cycle time line implement system requirements  practical application
 directive 93/42/EWG risk evaluation and for risk control
New functions in Qware Riskmanager 4.0
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In-Vitro-Diagnostics IVD FDA authorization CE-marking

Trial Version of Qware Riskmanager

product lifecycleQware Riskmanager In-Vitro-Diagnostics Medizinprodukte
Regualtory Affairs likelihood of appearing a damage  Medica 2011

Trial Version Qware Riskmanager

We and our customers are confident about the outstanding capability of Qware Riskmanager. For this reason we offer you a fully functional Trial Version of the market leading software for risk management according to DIN EN ISO 14971, IEC EN 60601-1-6 and DIN EN 62366.

Upgrading the trial version to a full version

After ordering the full version of Qware Riskmanager you will receive your individual key for clearing, which activates your Trial Version to a full version. Data which have already been entered can naturally be used any longer. So there is nothing to be said against testing the Trial Version with real project data which saves time and money.

Restrictions of the Trial Version

The Trial Version nearly contains the full scope of benefits as the full version. Only the print and export functions are limited. So you get a complete test environment for your risk management tasks. You can use the try out version up to 30 days. If you would like to expand the Trial Version time, don't hesitate to contact us.

Source of supply

You can get Qware Riskmanager via CD-Rom or you can download the Trial Version directly from this homepage.


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Qware Riskmanager 4.0
Qware Riskmanager 4.0
The market leading software solution for the riskmanagement of medical devices and in-vitro-diagnostics is completely revised.
Read more about the new functions of Qware Riskmanager 4.0
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Partner
Screenshots Qware Riskmanager Here you find the appropriate partner to implement your risk management system.
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