Memorable events don't just happen. A business event is the definable occurrence in our business scenario. Over the past few months, all the hard wor
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A panel discussion on ‘The Digital Opportunity’ offers the perfect platform to meet, interact and share ideas about how ‘digital’ is transforming t
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How to evaluate the performance of your text mining data? Precision and recall The presentation of the proposed method was evaluated in compari
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Pubrica, another brand established and owned by Guires, extends services to authors and publishers by providing services in the domain of medical and
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Guires, a leading player in the Indian market has recently made an entry into the UK market. Guires has under its aegis a brand ‘Pepgra’, which exclu
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Revised European guidance for medical devices have included comprehensive considerations relating to risk management, post-market surveillance and ha
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The Clinical Evaluation Report (CER) is a prerequisite document required to be submitted to regulatory bodies along with the technical file as a part
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European regulatory framework has established rules that govern the development, manufacturing, and marketing of medical devices in the European mark
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Clinical Evaluation Report (CER) comprises of three major parts that present complete clinical evaluation information of the medical device under con
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The Clinical Evaluation Report (CER) is an integral part of conformity evaluation of a medical device and the manufacturer’s needs to take into accou
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