Regulatory Compliance Does Not Need to Come at the Cost of Innovation and Development

For a number of years quality and regulatory affairs have been viewed as the stifling force against medical device development and innovation -and the new MDR updates throw this dynamic into even sharper relief. But this does not need to be the case! Now is the perfect opportunity for medical device companies to be proactive in their regulatory structures and adoption and move regulatory adoption compliance into the wider business strategy to create efficient and compliant development pathways.

The brand new Medical Device Clinical Pathways Forum is the only conference that is dedicated to ensuring your teams can comply with the multitude of regulations governing the development of medical devices and create a proactive regulatory strategy to manage you MDR adoption and audit pathways.

Are you currently struggling with:

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interpreting the new med dev and regulatory changes? baxter will show you how.

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Creating a clinical lifecycle management strategy under the new mdr? siemens will help you to align the regulatory landscape with your company’s clinical strategy.

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Integrating legacy devices into the new clinical evaluation framework? bactiguard share their top tips.

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Struggling to streamline and proactively manage your supplier relationships? hear how ferring and our delegation are managing this challenge in our interactive roundtables.

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Developing a tailored medical device compliance and oversite strategy? oticon and nimio will take you through the key steps and challenges.

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Evaluating your audit pathway options and preparation requirements for compliance? our interactive and personalised training day takes you through the best regulatory compliance strategies and ensures you are compliant with our mock inspection.

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