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A Question 30 Years in the Making: Would a Final LDT Rule Withstand Judicial Scrutiny?

FDA Law Blog

The PR first sets out to establish that it has authority to regulate in vitro diagnostic “test systems” as devices, and not just the system’s individual components, such as reagents, instruments, specimen collection devices, and software. Specific features of the PR will foreseeably yield new bases for challenge.

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Hospice in Prison Part 1: An interview with Michele DiTomas and Keith Knauf

GeriPal

We start off part one by interviewing Michele DiTomas, who has been the longstanding Medical Director of the Hospice unit and currently is also the Chief Medical Executive for the Palliative care Initiative with the California Correctional Healthcare Services. But now we have older people dying of older people illnesses. Michele: Yep.

Family 132
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HIV, Aging, and Palliative Care: Peter Selwyn and Meredith Greene

GeriPal

There was some at the time, which was 2006 so also, it’s been a while since the guidance has been updated and other guidance for other viral infections like hepatitis B and C. Eric 26:39 But I’m also hearing that 1 out of 10 newly diagnosed cases are not those individuals. Eric 18:33 Why did they do that?