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Ram is Quality Manager (Design & Development) at Planet Innovation. He has over 12 years' experience in the medical device and IVD industries in areas of Quality Assurance, Regulatory, New product development, R&D, Manufacturing and Lean/Six Sigma process improvements.
With the European Medical Device Regulations deadline looming, we look at the major changes impacting medical device manufacturers and the release of a few guidance documents by the European Commission.
