Remove topics drug-approvals
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The Importance of Semantic Search Capabilities for Life Sciences Orgs

Velocity of Content

For example, a query for “rare disease drug approval” would include results for the Orphan Drug Act from the FDA. Google recognizes that “drug approval” relates to “government regulations.” It also knows “orphan drug” and “rare disease” are associated, though different terms are used.

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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! Co-authored with Dinesh Thakur their book – The Truth Pill – The Myth of Drug Regulation in India was released this October. Book Review: ‘The Truth Pill: The Myth of Drug Regulation in India’.

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Balancing Innovation: India’s Views for Pharmaceuticals in the Efta Trade Deal

IIPRD

[iv] The outcome of these negotiations therefore can significantly impact the return on investment (ROI) for pharmaceutical companies, potentially influencing their willingness to invest in future drug development. Studies have established a correlation between TRIPS-plus provisions and increased drug prices in importing nations.

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IP Reveries: Class 5.1 – Drugs, Secrets, and Innovation: Brooding Over The Basics

SpicyIP

After a few sessions on conceptual and theoretical ideas around IP, this set of sessions will now take the class on a different not-so-theoretical topic and deliberates upon IP issues that crop up around clinical trial test data, drug innovation, Indian drug regulatory regulation etc. good morning. Confused face).

IP 118
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Journey Through “Augusts” on SpicyIP (2005 – Present)

SpicyIP

He wrote detailed posts on this topic later here and here. Talking about this topic, the issue of Judicial Recusals also shouldn’t be left untouched – an issue that has been the heart of several IP controversies, notably the Novartis dispute. Time and again, the issue of drug regulation has popped up.

IP 105
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FDA Testimony Before the U.S. Senate Regarding Reauthorization of the Biosimilar User Fee Act

LexBlog IP

The BsUFA is a law authorizing FDA to assess and collect fees from drug manufacturers that submit Biological License Applications for biosimilar products. The testimony spanned many topics, but notably the FDA discussed the progress of biosimilar approvals, including its impact on cost. decrease in price (for infliximab).

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Journey Through “Octobers” on SpicyIP (2005 – Present) 

SpicyIP

For context, these trials are conducted by pharmaceutical companies as R&D to, evaluate the efficacy, risks, and health benefits of new drugs/components. Access to clinical trial data not only helps drug innovation but also impacts consumer benefits and drug pricing. and Class 5.2 Read Anupriya’s excellent post here.