EP 16 Policy Development and Patient Engagement for Rare Disease with Alistair Kent

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Recorded06 Sep 2019

Publisheranchor.fm ↗

Handlerec:12123672

Show notes

This week on our podcast, we speak to Alastair Kent, a world leader in policy development and patient engagement for rare disease. In this episode, we discuss how research is changing in rare conditions and what part DNA sequencing and data sharing are playing in this.

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“What did the council decide on item 42?” — answered with the speaker and the moment.

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