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Joanne S. Eglovitch

Reporter

Indexed articles, last 90 days
13
Latest publication
Oct 1, 2026
Outlet visibility, for Raps
Top 1M sites
Earliest in this view
Aug 7, 2026

Latest articles

  1. Article · Oct 1, 2026 · Joanne S. Eglovitch

    ICMRA joins call to replace animal testing with alternative approaches (opens the original)

    Excerpt · Positive tone · English

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    The US Department of Health and Human Services on Wednesday announced a program and funding opportunity through the Advanced Research Projects Agency for Health (ARPA-H) called the Simulation-augmented, Real-time Platform Adaptive Seamless Trials (SURPASS) program. The program aims to transform how clinical trials are designed and conducted to streamline them and ultimately bring products to market sooner.

  2. Article · Aug 24, 2026 · Joanne S. Eglovitch

    FDA seeks feedback on framework for regulating GenAI devices (opens the original)

    Excerpt · English

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    Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug, and medical device regulation, and what we’re reading from around the web. This week, FDA said it wants to conduct research into perceived barriers to enrolling women in pregnancy exposure registries, the agency announced priority review voucher fees for the next fiscal year, and it named permanent leaders to three of its product centers.

  3. Article · Aug 24, 2026 · Joanne S. Eglovitch

    Therapeutic equivalence: FDA finalizes guidance on TE evaluations (opens the original)

    Excerpt · English

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    Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug, and medical device regulation, and what we’re reading from around the web. This week, FDA said it wants to conduct research into perceived barriers to enrolling women in pregnancy exposure registries, the agency announced priority review voucher fees for the next fiscal year, and it named permanent leaders to three of its product centers.

  4. Article · Aug 20, 2026 · Joanne S. Eglovitch

    FDA finalizes Q&A guidance on developing cell and gene therapies (opens the original)

    Excerpt · English

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    Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug, and medical device regulation, and what we’re reading from around the web. This week, FDA said it wants to conduct research into perceived barriers to enrolling women in pregnancy exposure registries, the agency announced priority review voucher fees for the next fiscal year, and it named permanent leaders to three of its product centers.

  5. Article · Aug 19, 2026 · Joanne S. Eglovitch

    Trump taps Heidi Overton as next FDA Commissioner (opens the original)

    Excerpt · English

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    Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug, and medical device regulation, and what we’re reading from around the web. This week, FDA said it wants to conduct research into perceived barriers to enrolling women in pregnancy exposure registries, the agency announced priority review voucher fees for the next fiscal year, and it named permanent leaders to three of its product centers.

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