![]() Various stakeholders (vendors, employees, auditors, etc.) can all collaborate together on DHF documents, checking them in and out of virtual vaults in a virtual workspace. ![]() With the help of virtual folders called Explorers, manufacturers can keep data of each department separate yet accessible. MasterControl also allows for quick search and retrieval of documents so that they are readily available to respective stakeholders for reference. Our design history files software solution is entirely Web-based, which allows authorized users from anywhere across the globe to remain connected in the entire document development lifecycle. ![]() MasterControl software, specifically tailored to meet manufacturers' DHF needs, is particularly useful in attaining and sustaining compliance with FDA, ISO, and CGMP regulations that are necessary for a device manufacturer's survival in business. ![]() To maintain precision when compiling design history files, manufacturers of Class 1 and Class II medical devices require the ability to build a comprehensive repository of all the design controls used in manufacturing their devices. MasterControl Design History Files (DHF) Software Facilitates Compliance
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