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BioWorld - Wednesday, December 17, 2025
Home » Topics » Regulatory

Regulatory
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USPTO wants to know: What happens when AI truly invents

Feb. 14, 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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USITC to investigate NASH trade secret fight

Feb. 14, 2023
By Mari Serebrov
The U.S. International Trade Commission (USITC) is launching an investigation into the importation from China of certain thyroid hormone receptor-beta agonists, products containing them and the manufacturing processes being used.
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Virtual IP display

Lots of changes coming to China IP scene, but improvement slow

Feb. 14, 2023
By Mari Serebrov
With China taking steps to enact or propose amendments to more than 60 intellectual property (IP)-related laws and regulations over the past few years, drug and device companies doing business in the country need to keep abreast of the changes. Despite China’s efforts, most of the participants in the Feb. 9 U.S. Patent and Trademark Office’s quarterly China IP webinar indicated in a pre-webinar survey that they have yet to see much of an improvement in China’s enforcement and regulation of IP rights.
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Regulatory actions for Feb. 14, 2023

Feb. 14, 2023
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Sunrise, Tasso.
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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.
Read More

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.
Read More

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.
Read More
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