USP 797.org
  

 

  Articles on USP 797   

USP 797 Home
How to Achieve USP 797 Compliance

JCAHO Schedule for USP 797 Implementation

Articles on USP 797

USP 797 2008 Guidelines

Purchase USP 797 Products

USP 797 Vendors

Q&A on USP 797

Contact Us

Articles on USP 797 

"Revising the Medicare Model Guidelines",
(c)
United States Pharmacopeia (USP), 2/06

In addition to creating the Model Guidelines, the Medicare Modernization Act also designates USP "to revise such classification from time to time to reflect changes in therapeutic uses of covered part D drugs and additions of new covered part D drugs." The links below provide additional information regarding USP's approach to the revision process.

First Revision to the USP Model Guidelines

As required under the Medicare Modernization Act, USP has revised the Medicare prescription drug benefit Model Guidelines. The revised Model Guidelines – Model Guidelines Version 2.0 – may be used by drug plans as they design their formularies for the 2007 benefit year.

Model Guidelines Expert Committee

The Model Guidelines Expert Committee is made up of expert volunteers and will be responsible for the Model Guidelines revisions.

Revision Process and Timeline

The revision process will, like the initial development process before it, be characterized by transparency, independence, and objectivity.

Public Comment

Any and all interested parties will have an opportunity to provide input into the revision process.

2005–2010 Model Guidelines Expert Committee Roster


What you will find on USP797.org : USP 797 regulations USP 797 vendors USP 797 products USP 797 articles USP 797 cleanrooms USP 797 barrier isolators USP 797 software
© 2005 USP 797.org / 59 West 19th St. : New York, NY  10011 : (212-463-0800) : info@usp797.org