ISO 14971 provides a framework for medical device manufacturers to identify and minimize risks through the design and manufacturing processes. Adhering to the standard helps ensure overall safety and ...

Risks to a medical device’s performance can occur at any stage of the product lifecycle, as highlighted at the 2015 Risk Management Summit conducted by AAMI. Sometimes, changes in a product may be so ...

Environmental contamination control is a crucial aspect of sterile pharmaceutical manufacturing, and risk management is needed to guarantee that the necessary control procedures are in place. The risk ...

As an advisor, assisting the organizations with managing and mitigating the risks of campus programs is important. We believe that taking time to learn the policies that guide risk management and ...

Our clients now need integrated strategic risk management guidance that addresses legal, business, technological and societal ...

Health care in the United States is stretched to its limit, and those who enter the medical field want to be able to provide the best care possible for their patients. For nurses, usually the backbone ...

Please define the meaning of “risk” from the perspective of environmental monitoring. Risk assessment consists of the identification of hazards and the analysis and evaluation of risks associated with ...

Risk management is the process of identifying potential risks and/or harms and creating a plan to prevent the risk from happening or reduce the risk as much as possible. There are different types of ...

Kovrr’s AI Risk Assessment and AI Risk Quantification modules highlight AI exposure.  Artificial intelligence (AI) used to be something that only existed in science fiction novels and dystopian movies ...

This document is intended to provide guidance to Purdue departmental areas that sponsor and are planning international travel. These best practices and procedures are not intended to be all ...