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  "documentTitle": "Nemaura Medical | Investor Presentation Deck | 22 slides",
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  "presentationDate": "2023-09-01 00:00:00",
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  "notes": "The slide outlines CE marking in Europe and the ongoing FDA PMA review process, including specific audit and inspection history.",
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      "text": "CE Approved Class 2b Medical Device in Europe\nFDA PMA submitted and in review\nFDA Bio-monitoring Division (BIMO) Audit conducted in December 2021 at Nemaura’s UK facility. A single 483 observation was issued. Company submitted a full and complete response to FDA in January 2022.\nFDA Pre-market inspection covering FDA’s Quality System/Current Good Manufacturing Practice regulations for Medical Devices (21 CFR Part 820) completed in Q2 2022. Full response sent and company continues dialogue in relation to the application. Further updates to be provided in due course.",
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      "text": "sugarBEAT® Regulatory Status",
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