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Indhold leveret af Darshan Kulkarni. Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af Darshan Kulkarni eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.
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Are CROs Losing Relevance in the Age of DCTs?

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Manage episode 446551801 series 3506216
Indhold leveret af Darshan Kulkarni. Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af Darshan Kulkarni eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.

In this episode, Isaac Rodriguez- Chavez and I discuss the impact of DCTs on sponsor relationships, CROs, and industry dynamics with the FDA.
We discuss,

1. How will DCTs impact sponsor relationships with CROs?

2. How do small CROs and sponsors adapt to emerging trends?

3. How do new trends impact industry relationships with the FDA?

4. Does DCT allows the FDA to advise sponsors?

5. What is the role of technology in DCTs?

6. How do DCTs reduce the cost of bringing drugs to the market?

7. What are the risks and advantages of DCTs?

8. What are the initial risks of DCTs?

9. Does the FDA even have jurisdiction over patient privacy?

Support the show

  continue reading

121 episoder

Artwork
iconDel
 
Manage episode 446551801 series 3506216
Indhold leveret af Darshan Kulkarni. Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af Darshan Kulkarni eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.

In this episode, Isaac Rodriguez- Chavez and I discuss the impact of DCTs on sponsor relationships, CROs, and industry dynamics with the FDA.
We discuss,

1. How will DCTs impact sponsor relationships with CROs?

2. How do small CROs and sponsors adapt to emerging trends?

3. How do new trends impact industry relationships with the FDA?

4. Does DCT allows the FDA to advise sponsors?

5. What is the role of technology in DCTs?

6. How do DCTs reduce the cost of bringing drugs to the market?

7. What are the risks and advantages of DCTs?

8. What are the initial risks of DCTs?

9. Does the FDA even have jurisdiction over patient privacy?

Support the show

  continue reading

121 episoder

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