• Compliance At Your Fingertips
  • Reduce Healthcare Acquired Infections
  • Save Time, Space & Money

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World's Most Complete Database Service of Manufacturers' IFU Documents

oneSOURCE gives your entire facility access to the world's most complete online database service of manufacturers' validated (IFUs). This means you can easily reduce errors in sterile processing and improve patient safety by subscribing to oneSOURCE.

Following the FDA regulated manufacturers' validated IFU document is essential for meeting AAMI Standards as well as CMS, Joint Commission & AAAHC accreditation requirements. Subscribing to oneSOURCE makes compliance practical and easy with value-added features like the one-page Tech Ready document that gives you the information you really need without scrolling through hundreds of pages.

Completely online and continuously updated, oneSOURCE also saves you time, space and money. No more bulky storage cabinets. No more costly staff-hours filing and updating IFUs. oneSOURCE is affordable and easily pays for itself. To learn more, play video or click Why oneSOURCE?

 

Efficient Management of Manufacturer Instruction for Use (IFU) Documents

Having access to current, validated manufacturers' Instructions for Use (IFU) documents is essential for facilitating safe and effective reprocessing of medical devices and equipment. If these processes are not carried out in accordance with the procedures outlined in the manufacturer's validated IFU, the items could pose a very real threat to the health and safety of both patients and staff. Typical failures to comply include improper cleaning, improper wrapping or loading in the sterilizer; incorrect reassembly of the device; and use of an incorrect sterilization process...click here to access the oneSOURCE White Paper.

 

 

Click to read 2015 Healthcare Purchasing News article "IFU's provide patient safety blueprint" - featuring oneSOURCE Document Management Services!

 

Joint Commission Safety Action:

The Joint Commission found improperly sterilized or high-level disinfected equipment as one of the top 5 non-compliant accreditation requirements and issued a Safety Action recommending that healthcare facilities make manufacturers' instructions available to all staff. oneSOURCE makes it easy for your entire facility to access thousands of manufacturers' IFUs 24/7. See the Joint Commission Safety Issue by clicking on the link.
 
 
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