Risk Management ISO 14971

Need support with getting your risk management file ISO 14971 compliant?

ISO 14971 Risk Management

Market access for your medical device and In vitro diagnostic 

Medical device companies must have established a risk management process that complies with ISO 14971. ISO ISO 14971 is formally recognized as the risk management standard by regulatory authorities in the US, Europe, Canada, Australia, and more. ISO 14971 improves your organization's ability to reduce uncertainty, and your ability to achieve the critical objective of ensuring device safety and effectiveness.

 

 

ISO 14971 helps your company with a systematic process to manage the risks associated with the use of a medical device and In vitro diagnostic. To maximize the effectiveness of your risk management system, ISO 14971 should be part of your quality management system (QMS) as required by ISO 13485. 

Our experts understand what it takes to manage process interactions to produce the desired outcome: patient safety. Qserve's team of RA/QA consultants can help you understand and comply with the requirements of the ISO 14971:23019  in global markets in an efficient, cost-effective way. 

Our services

Planning - Define the scope of risk management activities and integration with your QMS.
Documentation - Identify gaps and opportunities to improvement 
Risk Analysis - Helping manufacturers focus on and address risk management activities to effectively analyze the risk associated with their devices.
Post Market Surveillance (PMS) - Making risk management complete and ensuring PMS feeds into RM

Have Questions about what Qserve can do for your company? Please complete the form below

How do you want us to follow up with you?
 
How can we help you? Contact us