On January 7, 2025, the U.S. Food and Drug Administration (“FDA” or “Agency”) released a long-awaited guidance titled, “Communications From Firms ...

The Food and Drug Administration Feb. 5 released an alert notifying patients of a safety concern using diabetes devices such ...

In 2023, the Global Drug Of Abuse Testing Market accounted for USD 6.8 Billion and is expected to reach around USD 11.8 Billion in 2032. Between 2023 and 2032, Lawrence John Prudour +91 91308 55334 ...

In the United States, the biomedical industry encounters numerous regulatory challenges in conducting nonclinical and ...

News-Medical speaks with Jordi Labs’ about its recent achievements, alignment with FDA expectations, and strategic ...

Vitti Labs says the Food and Drug Administration erred in subjecting the lab's umbilical cord-derived product in a way that brings greater regulation. Liberty-based Vitti Labs, a human tissue bank ...

Verified Market Research® a leading provider of business intelligence and market analysis is thrilled to announce the release of its comprehensive report on the, "Medical Device Connectivity ...

Instructions for filling out the medical device establishment licence application. Information includes a calculation chart for the required fees and related guidance documents.

The Medicines and Healthcare products Regulatory Agency (MHRA) has unveiled comprehensive guidance to assist medical device manufacturers in navigating the upcoming Post-Market Surveillance (PMS) ...

“Our consumers and everyone in the food industry want and expect a strong FDA, and a consistent, science-based national regulatory framework. We have been saying for years that FDA is the ...