HeyJaredNick Paul Taylor
- Indexed articles, last 90 days
- 5
- Latest publication
- Oct 1, 2026
- Outlet visibility, for Raps
- Top 1M sites
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- Aug 10, 2026
Latest articles
Euro Roundup: Council of the EU adopts âpharma packageâ to advance legislative reform agenda (opens the original)
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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.
Asia-Pacific Roundup: TGA seeks feedback on automated decision making for changes to listed medicines (opens the original)
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Welcome to another installment of This Week at FDA, your weekly source for updates â big and small â on FDA, drug, and medical device regulation, and what weâre 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.
Euro Roundup: EMA seeks feedback on framework designed to drive uptake of data standards (opens the original)
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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.
Euro Roundup: Notified bodies call for access to Eudamed to enable move to risk-based oversight (opens the original)
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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.
Asia-Pacific Roundup: India establishes tougher penalties for filing misleading or fake documents (opens the original)
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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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