{"href":"http://player.captivate.fm/services/oembed?url=http%3A%2F%2Fplayer.captivate.fm%2Fepisode%2Fd3744d13-d3c1-4fef-8bea-14898ce9997d","version":"1.0","provider_name":"Captivate.FM","provider_url":"https://www.captivate.fm","width":600,"height":200,"type":"rich","html":"","title":"How Phagenesis Is Using Regulatory Affairs as They Develop a Treatment for Dysphagia","description":"How Phagenesis Is Using Regulatory Affairs as They Develop a Treatment for Dysphagia with Rebecca Sheridan\n\nWhat if regulatory affairs were not only viewed as a necessary burden, but actually help a medical device company? Our guest today thinks that is exactly the case. \n\nPhagenesis, a greenlight.guru customer, is a new type of medical device startup company with a fascinating story. Their products are transforming the lives of people with dysphagia by restoring neurological control of swallowing. Nestl\u00e9 recently struck a deal to acquire Phagenesis as reported by The WSJ.\n\nToday Jon is talking with Rebecca Sheridan, Head of Quality Assurance and Regulatory Affairs at Phagenesis. Join us as Rebecca shares more about her background, the Phagenesis story and the role of regulatory affairs in the medical device industry. \n\nSome of the topics discussed today include:\n\n\u25cf\tRebecca\u2019s professional background\n\u25cf\tDifferences between large and small medical device companies and joining Phagenesis\n\u25cf\tInvolving the whole team in regulatory affairs to make it work for everyone\n\u25cf\tUsing greenlight.guru as a tool at Phagenesis\n\u25cf\tAdvice for medical device startups\n\u25cf\tOverview of Phagenesis and dysphagia treatments","thumbnail_width":300,"thumbnail_height":300,"thumbnail_url":"https://artwork.captivate.fm/501b37b5-d1c7-41d2-9746-fc05449e9bae/a54fc408-9b92-4337-a079-1bc0726085c8.jpg"}