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Pfizer to deepen cost cuts as latest sales forecasts miss expectations

BioPharma Drive: Drug Pricing

The company is now expecting to save $4 billion by the end of 2024, with a majority of the spending cuts coming from drug research and development.

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Drug Channel Implications of the Inflation Reduction Act (NEW Live Video Webinar)

Drug Channels

Fein, president of Drug Channels Institute (DCI) and the author of Drug Channels , invites you to join him for DCI’s latest live video webinar: Drug Channel Implications of the Inflation Reduction Act This event will be broadcast live on Friday, April 5, 2024, from 12:00 p.m. to 1:30 p.m. All rights reserved.

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Distinguishing the Roles of Preclinical vs. Clinical CROs in Clinical Research

Vial

In this article, we will define preclinical and clinical CROs, as well as highlight the unique needs and challenges of these organizations in their respective stages of drug research. between 2024 and 2030. between 2024 and 2030. What is a Pre-Clinical CRO? billion in 2022 and is projected to reach US$10.2

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ACTO EXPANDS INVESTMENT IN ARTIFICIAL INTELLIGENCE TO SOLVE UNMET NEEDS IN THE LIFE SCIENCES INDUSTRY

ACTO

The life sciences industry is actively looking for new ways to leverage AI to bring drugs to market faster to patients waiting in need,” said Parth Khanna, CEO of ACTO. Current solutions are almost exclusively focused on marketing, HCP targeting, workflow automation, and performance insight.

Science 52
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Article FDA Thank You FDA’s new guidance explains what to do during a BIMO inspection

Agency IQ

BY LAURA DIANGELO, MPH | JUN 5, 2024 5:35 PM CDT Background: The FDA’s Bioresearch Monitoring (BIMO) program In FDA’s words, the BIMO program is “a comprehensive program of on-site inspections, data audits, and remote regulatory assessments designed to monitor all aspects of the conduct and reporting of FDA regulated research.”

FDA 40
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Article EMA Thank You What we expect European regulators to do in August and September 2024

Agency IQ

What we expect European regulators to do in August and September 2024 In this recurring feature, AgencyIQ, through public data and previous analysis, determines what European medicine and device regulators will likely do in the month ahead, including key deadlines, meetings, events, planned regulations, comment periods, and more.

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Article EMA Thank You What will the orphan drug market exclusivity haircut mean for industry?

Agency IQ

The problems: Although the current regulation stimulated orphan drug research, it didn’t do enough The regulation fostered development of medicines for rare diseases since implementation, but not enough. Parliament will be elected in 2024, which could further slow down the process. Additionally, a new E.U.