Remove topics regulatory-requirements
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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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Key Trends in the Shifting World of Search

Velocity of Content

Also, info pros can contribute to initiatives within their organizations to create institutional guidelines on the use of AI, working with stakeholders from IT, legal, regulatory, research, and data science groups to ensure that AI tools are built with reliable, licensed content.

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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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Utilizing RightFind Across the R&D Pipeline

Velocity of Content

In RightFind, reseachers and investigators can analyze previously published studies and create reviews of articles pertaining to a topic, such as a specific disease, chemical compound, or ingredient. Regulatory. Scientific literature plays a critical role in the regulatory submission cycle. Patent Validity. Medical Affairs.