
ALT The FDA has a proposed ruling (FDA-2023-N-2177-0001) to amend its regulations to make explicit that in vitro diagnostic products (IVDs) are devices under the Federal Food, Drug, and Cosmetic Act (FD&C Act) including when the manufacturer of the IVD is a laboratory. The PASCV along with multiple other microbiology and healthcare organizations and societies vehemently opposes this proposed ruling. Below, you will find the link to the letter sent as the official stance of the PASCV as an organization. We ask that you get involved as this directly affects all of us. 1. Please click on this link to place a public or anonymous comment against this proposed ruling. https://www.regulations.gov/commenton/FDA-2023-N-2177-0001 2. Please click this link to determine your federal representative and let them know you oppose this proposed ruling. https://www.house.gov/representatives/find-your-representative





























