Ensuring that components (parts) are free from contamination is becoming increasingly important in the medical device industry. Problems caused by inadequate or improper cleaning can harm patients and ...

We collaborate with the world's leading lawyers to deliver news tailored for you. Sign Up for any (or all) of our 25+ Newsletters. Some states have laws and ethical rules regarding solicitation and ...

Medical device manufacturers use cytotoxicity testing to help prove that devices that come into contact with the human body are biocompatible. Testing results are critical for gaining market access, ...

Please provide your email address to receive an email when new articles are posted on . The FDA has announced a proposed rule that would require manufacturers of talc-containing cosmetic products to ...

The American Architectural Manufacturers Association (AAMA) has released an updated document specifying test methods, specifications, and field checks used to evaluate the structural adequacy of wall ...

A new National Academies of Sciences, Engineering, and Medicine report provides an overview of new approach methods in human health risk assessment of chemicals, and calls on the U.S. Environmental ...

The U.S. Food and Drug Administration announced Thursday that it will be phasing out a requirement that monoclonal antibodies and other drugs be tested on animals, saying in a news release that there ...

The Food and Drug Administration said today it is abruptly withdrawing its proposed rule that would have created approved, standardized testing methods for detecting and identifying cancer-causing ...

Agricultural soil testing is critical to determining soil’s nutrient concentration and variability across your fields. It is ideal to test your fields’ soil at least every two to three years to inform ...