Fish & Richardson Trademark & Copyright Thoughts

DECEMBER 2, 2020

As of the date of publication, 36 states and the District of Columbia have legalized cannabis for medical use, while 15 states and the District of Columbia have legalized it for adult recreational use. FDA Regulation. The FDA approved its first drug containing CBD as an active ingredient, Epidiolex, in 2018. THC from Schedule I.

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Fish & Richardson Trademark & Copyright Thoughts

FEBRUARY 4, 2021

With this milestone on March 23, 2020, insulin and other biological products previously regulated as “drugs” transitioned to regulation as biologics, paving the way for increased biosimilar diversity. Biosimilar Drug. Below, we review these notable developments and more from 2020. Biosimilars Approved as of 2020.

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Indiana Intellectual Property Law

MARCH 7, 2024

Patent Office issued the following 312 patents to persons and businesses in Indiana in January 2024: Patent Number Patent Title US 11886208 B2 Electronic user interface for electronic mixing of water for residential faucets US 11884752 B2 Inhibited non-pregelatinized granular starches US 11883335 B2 Medical products storage (..)

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LexBlog IP

NOVEMBER 9, 2023

Centralizing governance of AI will enhance your ability to follow the rapidly-changing regulations and guidance issued by both state and federal regulators and implement a compliance program to respond to the changing landscape. The healthcare industry is heavily regulated; compliance is no stranger to it.

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LexBlog IP

JANUARY 22, 2022

Trademarks are the very embodiment of the nature and character of a product or service. For example, it is illegal to import, sell, distribute, or manufacture pharmaceuticals in Nigeria without first securing a product registration from the National Agency for Food and Drug Administration and Control (NAFDAC). Thank you, Lara.

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LexBlog IP

JANUARY 22, 2022

Trademarks are the very embodiment of the nature and character of a product or service. For example, it is illegal to import, sell, distribute, or manufacture pharmaceuticals in Nigeria without first securing a product registration from the National Agency for Food and Drug Administration and Control (NAFDAC). Thank you, Lara.

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Fish & Richardson Trademark & Copyright Thoughts

JANUARY 11, 2022

Biosimilar Drug. In 2021, regulatory agencies focused on three interrelated issues: (1) decreasing anti-competitive behavior in the biosimilars space, (2) lowering biologic drug prices, and (3) providing further guidance to clarify the regulatory pathway for biosimilars. Tackling Biologic Drug Pricing. Reference Product.

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