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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).