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Follow on Google News | ![]() SARACA reduces CER development time by up to 40% with best practices tracker toolGrowing experience producing Clinical Evaluation Report updates leads to highly-effective and cost-efficient methods that benefits clients
By: Saraca Solutions "Our team's deep experience in international medical device regulatory issues has led to creating these best practices for the benefit of our clients who depend upon us for this reporting compliance," Saraca Solutions, he said, developed a method of grouping specific experts to collaborate. This led to the development of a unique AI-based tool that automates some of the research and collection work, particularly for relevant article searches, which reduces tasks that typically take nearly 15 hours down to about one hour. A CER documents conclusions for a medical device's clinical evaluation and consists of analyzed clinical data collected from either investigation of a company's device or studies of substantially equivalent devices. Required for all medical devices marketed in Europe, the CER demonstrates that the device achieves its intended purposes without additional risk. Learn more by visiting saracasolutions.com (http://www.saracasolutions.com/ For more information, contact: Kevin J. Berger, Head of Marketing +1-612-237-9122 Kevin.berger@ Skype: kevinjberger OR Kuldeep Tyagi, CEO and Managing Director +1-901-286-1890, +91-9711612068 kuldeep.tyagi@ Skype: tyagi_k75 End
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