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Category: FDA
Oxygen Transfillers: Important Upcoming Deadlines You Need to Know
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
FDA Annual Records Review
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
FDA, DOT Accreditation Training with Applied
We will be hosting live streams and in-person FDA, DOT seminars in 2024! Topics include how to handle, transport and fill oxygen and other accreditation topics to help home care providers keep up with changing regulatory and technical
FDA Drug Reporting under the CARES Act
The FDA CARES Act mandates that all drug manufacturers (including medical oxygen transfillers) report specific details about their drug volumes to the
It's FDA Renewal Time!
Transfillers need to annually renew their transfilling locations and drug listings with the FDA. Here are some quick tips to help you stay
New FDA Drug Reporting Service
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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