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As Document Control and Audit Management are key requirements in complying with life science industry regulations, Cambridge based medical device manufacturer, Biochrom Ltd has chosen a compliance management solution from Gael Ltd to improve the efficiency and effectiveness of the company’s internal document and audit management system. The award-winning compliance management software, Q-Pulse, will not only identify and address corrective and preventive actions within the company, but also help establish a framework to maintain and improve how quality activities are managed. Now in its 40th year, Biochrom’s products are sold internationally to a wide range of applications in the clinical, life-science and industrial markets. Martin Ellis, Quality Manager at Biochrom said: ‘Q-Pulse will be of substantial help to us in managing our regulated actions and activities in line with key regulations within the life science sector such as ISO standards and the FDA’s 21 CFR Part 11. ‘An extremely important part of these regulations is documentation and every aspect of our processes, activities, and operations must be documented. Managing these requirements with an electronic system such as Q-Pulse is invaluable for us, whilst also helping us maintain and improve both our procedures and the processes on which they are built.’ For further information please contact:
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