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7 ways to challenge FDA’s regulation of LDTs
Manage episode 405521517 series 3506216
Treść dostarczona przez Darshan Kulkarni. Cała zawartość podcastów, w tym odcinki, grafika i opisy podcastów, jest przesyłana i udostępniana bezpośrednio przez Darshan Kulkarni lub jego partnera na platformie podcastów. Jeśli uważasz, że ktoś wykorzystuje Twoje dzieło chronione prawem autorskim bez Twojej zgody, możesz postępować zgodnie z procedurą opisaną tutaj https://pl.player.fm/legal.
The FDA's announcement of its intention to regulate Lab Developed Tests (LDTs) in line with medical device regulations has sparked concerns among developers, anticipating significant financial implications.
We provide a comprehensive overview of seven strategic approaches for LDT developers to challenge the FDA's regulatory proposal.
Firstly, leveraging the public comment period,
Participating in Part 15 hearings provide direct avenues to voice concerns and influence final regulations,
Additionally, joining industry associations allows for collective lobbying efforts on behalf of developers,
Exploring legal challenges, though potentially premature without final action, remains an option,
Raising public awareness through media campaigns is suggested, emphasizing the benefits of LDTs and drawbacks of proposed regulations.
Collaboration with healthcare providers to gather real-world evidence and testimonials strengthens the developers' case.
Lastly, engaging in congressional lobbying harnesses legislative power to potentially alter or block the FDA's proposals.
Despite the FDA's focus on patient safety, developers are presented with a multi-pronged approach to effectively challenge and shape the outcome of the regulatory process.
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