risk-analysis, DIN 14971, risk-management, medical-devices
Risko analysis, DIN 14971, Risk management Medical devices, In-Vitro-Diagnostics, IVD DEUTSCH | IMPRINT 15.05.2008 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 normQware Riskmanager
ISO 9000 implementing of a Risk analysis risk control
post production information implementation of risk management according to DIN EN 14971- Advantages
risk management versus Risk analysis documentation- Screenshots
seminars post production information risk management report- Tryout
DIN EN ISO 14971 In-Vitro-Diagnostics CE-marking- Full version
FDA authorization CE-marking- Download
Qware Riskmanager- Purchase
product lifecycleRisk analysis of medical devices post production information- FAQ
harmonized norm DIN EN 14971
accomodation certification notified bodyReferences
implementation of a risk analysis risk management normative law regulations
Likelihood and severity evaluation after measuresPartner
DIN EN ISO 14971:2000
assignment with DIN EN ISO 13485_2003Articles | Reports | News
product process severity measures evaluation likelihood
life cycle time line implement system requirements practical applicationService
directive 93/42/EWG risk evaluation and for risk control
New functions in Qware Riskmanager 2.5
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In-Vitro-Diagnostics IVD FDA authorization CE-marking

Tryout of Qware Riskmanager - risk analysis under DIN 14971

product lifecycleQware Riskmanager In-Vitro-Diagnostics Medizinprodukte
Regualtory Affairs likelihood of appearing a damage  New functions

Tryout Qware Riskmanager

We and our customers are confident about the outstanding capability of Qware Riskmanager. For this reason we offer you a fully functional tryout version of the market leading software for risk management according to DIN EN ISO 14971.

Upgrading the tryout to a full version

After ordering the full version of Qware Riskmanager you will receive your individual key for clearing, which activates your tryout 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 tryout version with real project data which saves time and money.

Restrictions of the tryout version

The tryout 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 20 times. If you would like to expand the tryout time, don't hesitate to contact us.

Source of supply

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


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