GMP: FDA publishes List of Guidance Documents for Medical Devices
02.11.2011
The FDA published a list in the Federal Register presenting documents regarding the regulation of medical devices which are to be considered for development in the fiscal year 2012 (October 2011- September 2012). The reason for the creation of this list is based on negotiations over the reauthorisation of the Medical Device User Fee and Modernization Acts (MDUFMA).
The source of the news: http://www.gmp-compliance.org/eca_news_2821_7128.html
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