Learning / Medical device / Page 3
On January 31, 2020, the UK formally left the EU. The post-Brexit transition period ended on January 1, 2021. Medic...
Read MoreA clean room for medical devices is created and maintained so that no dust, bacteria, or contaminants can enter. To...
Read MoreBoth in terms of income and employment, the Indian healthcare industry has grown to be one of the country's biggest...
Read MoreA new group of regulators at various levels should be established, according to the Parliamentary Standing Committe...
Read More‘PPE’ is usually well known as Personal Protective Equipment. PPEs is an essential apparatus, specially designe...
Read MoreAs per the draft guidelines laid down by FDA (Food and Drugs Administration), “Remanufacturing” is defined as t...
Read MoreGlobal regulatory organizations want evidence that the medical equipment that is manufactured by the medical indust...
Read MoreQMS stands for Quality Management System, is an organized system consisting of method and actions that includes Sup...
Read MoreDrugs, vaccines, and medical devices are the three essential industrial foundations of contemporary healthcare tech...
Read MoreArtificial intelligence, also known as AI, is a technology that is regarded as being transformative in the digital...
Read MoreThe outcomes of a clinical examination of your medical device are documented in a Clinical Evaluation Report (CER)....
Read MoreMedical devices developed for human use are used for either diagnosis or treatment. They could be a device, an appl...
Read MoreThe MDR is a comprehensive revamp of medical device regulation in Europe with the goal of enhancing quality and saf...
Read MoreThe COVID-19 pandemic has compelled the medical device and IVD industry to think of innovative, creative ways to sa...
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