A new Food and Drug Administration AI tool that could speed up reviews and approvals of medical devices such as pacemakers and insulin pumps is struggling with simple tasks, according to two people ...
Single-use medical devices (SUDs) and sustainable practices are not mutually exclusive, but finding common ground is not a simple proposition. There is no question that SUDs have contributed to ...
Get the latest federal technology news delivered to your inbox. Two Democratic lawmakers are looking to establish standardized policies and transparency requirements for the use of electronic medical ...
In conversations about medical device cybersecurity, attention focuses on the Food and Drug Administration’s (FDA) rules and guidelines. With a refresh in 2023 that emphasized new protocols for ...
Medical equipment and devices play an essential role in most patient interactions. The MedTech industry is driven by evolving regulations, digital transformation, data analytics, artificial ...
Power management is a primary design constraint in portable medical devices because functional demands continue to grow ...
India Education Diary on MSN
Steps to regulate the pricing and quality of medical devices
India, Feb. 3 -- The National Pharmaceutical Pricing Authority (NPPA) under the Department of Pharmaceuticals (DoP) fixes ceiling prices of medicines included in the National List of Essential ...
Device Makers are currently at an intersection of accelerated innovation and heightened regulatory scrutiny. Regulatory affairs stands in the center guiding operational resilience and a coherent ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results