risk-analysis, DIN 14971, risk-management, medical-devices
Risko analysis, DIN 14971, Risk management Medical devices, In-Vitro-Diagnostics, IVD DEUTSCH | IMPRINT 24.06.2016 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
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
In-Vitro-Diagnostics IVD FDA authorization CE-marking

Download of Qware® Riskmanager 7.0

product lifecycleQware Riskmanager In-Vitro-Diagnostics Medizinprodukte
Regualtory Affairs likelihood of appearing a damage  Qware® Riskmanager

Download the Trial Version of Qware® Riskmanager

Here you can request a download link for the free Trial Version of Qware® Riskmanager.

Please take notice that downloading the Trial Version will not cause any costs for you, it will not create any obligations and your personal data will not be referred to anyone.

Title
First name*  
Last name*
Company*  
Department
Street*
Postal code*
City*
Country
E-mail*
Phone*
Fax
Subscribe to Newsletter.
 
Fields marked by * are mandatory
 8.2.0
Qware® Riskmanager
A new version of the market-leading software solution for generating technical documentation for medical devices and in-vitro-diagnostics has been released.
Read more about the new functions of Qware® Riskmanager
Downloads
Further information
about the Qware® Risk-
manager as download:
References
Trial Version
Screenshots
Screenshots Qware® Riskmanager
top of page