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Pharma and medical device regulation – GTDT – Lexology

Olartemoure Blog

We touch on topics like its regulatory framework, clinical practice, marketing authorization, amending authorizations, recall, promotion, enforcement of advertising rules, pricing and reimbursement, off-label use and unlicensed products, sale and supply, and recent trends that have been noticed.

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I Filed an Amicus Brief Against New York’s Editorial Transparency Law

Technology & Marketing Law Blog

General Business Law Section 394-ccc, the 2022 law that requires social media platforms to disclose their editorial policies towards “hateful conduct.” It is definitely counterintuitive to oppose transparency requirements due to our strong regulatory and social norms in favor of transparency.

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Provisional refusal in Colombia

Olartemoure Blog

A provisional refusal is an initial statement from the local trademark office indicating that the application does not meet certain legal requirements. It provides the applicant with an opportunity to defend their case before a final decision is made. Don’t let it block you! Act fast with our support.

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Book Review: ‘The Truth Pill: The Myth of Drug Regulation in India’

SpicyIP

We are thrilled to review Prashant Reddy’s new book on the Indian drug regulatory system! Given that drug regulation has a direct nexus to public health, maybe even more than patents, several years ago, Shamnad, Prashant and Sai started a new initiative on SpicyIP to throw more light on India’s drug regulatory framework.

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My IP Intensive Experience: From Seminars to CIPO and Beyond

IPilogue

This article was written as a requirement for Prof. The IP Intensive starts with a 2 week seminar series where students are exposed to a variety of IP related topics, followed by a 10 week placement at an organization to allow students to gain working experience. Pina D’Agostino’s IP Intensive Program.

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Biden administration releases wide-ranging executive order on AI

LexBlog IP

In the coming weeks, we will dive deeper into critical topics covered by the new EO. The White House aims to establish comprehensive regulatory principles over the AI industry. Manage risks in federal AI use and enhance regulatory capacity for better results.

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A Place Where Science Business Meet: My Internship Experience at AstraZeneca Canada

IPilogue

As part of the course requirements, students were asked to write a reflective blog on their internship experience. I was pleased to gain exposure to a variety of topics including patent litigation, pharmaceutical regulations, and privacy law over the course of my internship.

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