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This course will teach you how to start making informed decisions with regards to meeting the requirements of the EU Medical Devices Directives. On completion of the training, participants will be able to identify the steps required to reduce the risks and uncertainty in the EU regulatory process and thus save time bringing products to the EU market.
This training course is HRDF approved under the SBL scheme.
On completion, you will be awarded an internationally recognized BSI Training Academy certificate.
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