This document provides a high-level overview of the new EU MDR requirements for manufacturers and an outline of RCA’s new EU MDR Compliance and MDR Implementation Services based on these requirements.
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Regulatory Compliance Associates® Inc. (RCA) provides worldwide services to the pharmaceutical, biologic, sterile compounding, biotechnology, and medical device industries for resolution of compliance and regulatory challenges.
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This document is to provide a high-level overview of the EU MDR requirements for manufacturers and an outline of RCA’s EU MDR Compliance and MDR Implementation Services based on these requirements. Both existing and new clients may be targeted as part of the marketing campaign for these new services. Download the full document below.
