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BioWorld - Tuesday, April 14, 2026
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Regulatory
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Regulatory actions for Feb. 14, 2023

Feb. 14, 2023
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Exelixis, Gracell, Iaso, Ironwood, Jubilant, Nrx, Ocuphire, Pfizer, Pharmazz, Sairopa.
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Website of The Federal Trade Commission

FTC adopts more strident tone in revised version of health products compliance guide

Feb. 13, 2023
By Mark McCarty
The U.S. Federal Trade Commission (FTC) has updated a 1998 compliance guidance for health care products, much of which reiterates the provisions of the legacy edition. However, this updated version calls for randomized, controlled clinical trials to substantiate any claims made in connection with medical devices. 
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US FDA looks to expand transparency to adcom guest speakers

Feb. 13, 2023
To increase transparency at its advisory committee (adcom) meetings, the U.S. FDA is proposing asking guest speakers to voluntarily disclose their financial interests and professional relationships to determine their eligibility to give a presentation at an adcom meeting.
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USPTO wants to know: What happens when AI truly invents

Feb. 13, 2023
By Mari Serebrov
With an eye toward the future, the U.S. Patent and Trademark Office (USPTO) is seeking comment on artificial intelligence (AI) technologies and inventorship issues that may arise as AI takes on a bigger role in innovation.
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Regulatory actions for Feb. 13, 2023

Feb. 13, 2023
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Anavasi Diagnostics, Concept Medical, Hyperfine.
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Regulatory actions for Feb. 13, 2023

Feb. 13, 2023
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Everest, GSK, Phathom.
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Toy bulldozer moving FDA letter blocks

OUS device makers on FDA’s short list for warning letters

Feb. 10, 2023
By Mark McCarty
It may still be true that a majority of medical devices are manufactured in the U.S., but that doesn’t stop the FDA from dropping a warning letter on facilities located outside the U.S. (OUS). In one of these warning letters, Microvention Inc., of Aliso Viejo, Calif., received a warning letter for its plant in Costa Rica, although the FDA waited until the second week of February to post the Sept. 30, 2022, warning.
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Regulatory actions for Feb. 10, 2023

Feb. 10, 2023
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Catalyst Orthoscience.
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Regulatory actions for Feb. 10, 2023

Feb. 10, 2023
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alvotech, Bellerophon, Medicinova, Mesoblast, Regeneron.
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Bills aimed at US drug pricing advance in Senate

Feb. 9, 2023
By Mari Serebrov
U.S. drug prices continue to be in the crosshairs of Congress, with the Senate Judiciary Committee once again sending five bipartisan bills targeting anticompetitive pricing tactics to the full Senate Feb. 9 with do-pass recommendations.
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