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 ...

The findings show that 93% of respondents worldwide now believe the number of crises is rising, a three percentage point ...

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 ...

According to Lockton’s report Risks for Food Manufacturers and Producers: Why Risk Management Is Now a Boardroom Issue, ...

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 ...

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 ...

This is underscored by ASIC’s 2025–26 Corporate Plan, which identifies both the use of AI and directors’ conduct as focus areas. It is clear that responsible AI adoption, strengthened governance, and ...

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 ...