It is key for medical device manufacturers to understand how the new MDR affects the conduct of clinical investigations, the collection and collation of efficacy and effectiveness data, and clinical reporting. The impact on organisations and stakeholders alike is immense as the new regulations are reshaping the wound care research arena.

See this article as to how eKare Inc and Real Healthcare Solutions Ltd. are working together to support their medical devices industry clients to align their clinical data strategy to meet the necessary clinical evidence requirements

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