The direct participation of the
pharmaceutical industry, and other interested stakeholders, in USP’s
Monograph Modernization Program is encouraged to assist in providing
updated public standards vital to strengthen efforts for both FDA and
USP to protect the public health. Paramount to this effort is the
submission of updated analytical methodology pertinent to a compendial
article, as well as materials which could be used for independent
validation. FDA encourages all stakeholders to fully support this
effort.
Further information to become an active participant in this process is available on USP’s website at http://www.usp.org/usp-nf/development-process/monograph-modernization. Additionally, information, to include periodic status reports on this effort, is available at http://www.usp.org/usp-nf/key-issues/monograph-modernization. (From USFDA)