The July 31st recommended deadline for 2024 CARES Act Drug Reporting is approaching fast. Here's what you need to know to stay compliant for 2024 and
So, if the FDA considers you a drug manufacturer, what does that mean? It means that you must take specific steps to ensure your patients receive the accurate purity of oxygen, and the FDA will verify your compliance with these procedures. One of those things is the annual records
Medical oxygen is an essential resource in the healthcare industry and is used to treat a wide range of respiratory conditions. To ensure the safety and quality of medical oxygen, there are specific label requirements that must be followed for high-pressure and liquid oxygen
Applied Home Healthcare Equipment, a long-trusted resource for oxygen filling, technical and regulatory support for DME and HME providers, has announced the launch of their new drug reporting
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