If drug tariffs don’t work, they could result in higher prices for American patients and increase drug shortages. Testing ...

DexCom received a warning letter from the Food and Drug Administration following inspections of two of its plants.

THE Food and Drug Administration (FDA) has launched an online application process for Certificate of Medical Device Notification (CMDN) for Class A ...

Dublin, Feb. 25, 2025 (GLOBE NEWSWIRE) -- The "What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained" training has been added to ResearchAndMarkets.com's offering.

Chemicals such as titanium dioxide and potassium bromate, whose safety has been debated, are allowed in foods in the United ...

along with the applicable quality management systems. Imricor is executing a modular review process with the FDA, whereby ...

The FDA cited issues with DexCom’s response to prior inspection findings, known as Form 483 observations. The inspections took place at the San Diego facility between October 21 and November 7, 2024, ...

Dublin, Feb. 25, 2025 (GLOBE NEWSWIRE) -- The "What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained" training has been added to ResearchAndMarkets.com's offering. This ...

To be a person in the year 2025 is to encounter, in one way or another, the marketing onslaught for compounded ...

The company does not expect the warning letter to materially impact its manufacturing capacity, sales or ability to seek ...

and Mesa, Ariz. related to concerns about manufacturing processes and quality management systems. The FDA cited issues with DexCom's response to prior inspection findings, known as Form 483 ...