Overview The Site Master File (SMF) is prepared by pharmaceutical manufacture and it should contain specific information about quality polices and activities of the site, the production and/or quality control of pharma manufacturing activities at site. SMF Should provide the clear information on the manufacturer's good manufacturing practices (GMP) related activities that can be useful for planning and for GMP inspection by regulatory authorities. SMF should be part of documentation belonging to the quality management system (QMS) of manufacturer and kept updated. SMF contain sufficient information however possible not exceed 25-30 pages plus appendices or attachments.The SMF should be part of documentation belonging to quality management system of the system of the manufacturer and kept updated accordingly. It should be regularly review to ensure that it is up to date. Content of Site Master File : General information on the manufacture Contact information on...