Our client is currently seeking a highly efficient Quality Management System (QMS) and ISO 13485 documentation for their Class-1 medical device, which has successfully undergone both clinical assessment and the registration process. However, in order to ensure its deployment in the real world, a robust QMS is imperative. To accomplish this, we are in need of an expert regulatory professional who can collaborate directly with the client to produce the necessary documents. While numerous templates are readily accessible online, it is crucial to have the guidance of seasoned experts who possess their own specifically tailored documents. Should you possess the expertise required, please do not hesitate to inform us of your availability to assist the client.
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