Biotech Catalyst Daily — FDA & Clinical Trial Intelligence

The catalyst calendar for investors allocating against FDA decisions.

Burns Media

If you also ran to check your prescriptions after listening to this episode, use our “Rx Inspector” tool to look up where your generic drugs were made: https://propublica.org/rx-inspector

#FDA #Medicine #Health #Safety #Drugs

Where Was My Generic Prescription Drug Made? - Rx Inspector - ProPublica

The FDA won’t tell Americans where their generic drugs are made, so ProPublica did it instead. Use information on your prescription label to locate the factory and see inspection reports.

ProPublica

For years, the FDA told the public that generics are just as safe and effective as brand-name medications. But ProPublica reporters found that this isn’t always true.

Listen to the first episode of “Paper Trail,” our new podcast. Subscribe: https://www.propublica.org/podcast/what-fda-wont-tell-you-generic-drugs-safety?utm_source=mastodon&utm_medium=social&utm_campaign=mastodon-post

#Podcast #Audio #FDA #Medicine #Health #Safety #Drugs

States

The latest news and headlines, featuring real time updates for countries, cities, states, politics, economy, sports, food, culture via Ken's Blogspot

World Capitals

The latest news and headlines, featuring real time updates for countries, cities, states, politics, economy, sports, food, culture via Ken's Blogspot

FDA RECALL
Brand: Blackstone
Product: Parmesan Ranch seasoning
Issue: Potential Foodborne Illness - Salmonella
Date: 05/15/2026
More: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/blackstone-products-recalls-parmesan-ranch-seasoning-because-possible-salmonella-health-risk #FDA #recall
Blackstone Products Recalls Parmesan Ranch Seasoning Because of Possible Salmonella Health Risk

Blackstone Products of Providence, Utah is voluntarily recalling certain lots of Blackstone Parmesan Ranch seasoning products because they have the potential to be contaminated with Salmonella. Blackstone’s action is based on a California Dairies, Inc. recall of dry milk powder due to potential Sal

U.S. Food and Drug Administration
FDA RECALL
Brand: Straus Family Creamery
Product: Various Ice Cream Products, pint and quart sizes
Issue: Presence of metal fragments
Date: 05/15/2026
More: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/straus-family-creamery-voluntarily-recalls-select-flavors-organic-ice-cream-due-potential-presence #FDA #recall
Straus Family Creamery Voluntarily Recalls Select Flavors of Organic Ice Cream Due to Potential Presence of Foreign Material

May 14, 2026; Petaluma, CA; — Straus Family Creamery is voluntarily recalling a small number of production runs of select flavors and sizes of its Organic Ice Cream due to the potential presence of metal foreign material. Only the production runs (noted by the “best by” date on package) specified l

U.S. Food and Drug Administration

📰 BIOTECH CATALYST

Regenxbio outlines accelerated approval path for RGX-202

This could position Regenxbio as a leader in gene therapy for…

In today's briefing →
https://burns-media.com/biotech/archive/2026-05-15?utm_source=mastodon&utm_medium=social&utm_campaign=biotech_resurface

#Biotech #FDA

World Capitals

The latest news and headlines, featuring real time updates for countries, cities, states, politics, economy, sports, food, culture via Ken's Blogspot

US Top News and Analysis | Bristol Myers Squibb turns to China to develop new drugs in newest cross-continent collaboration

AI generated summary, Read the full article for complete information.

Bristol Myers Squibb announced a multi‑billion‑dollar partnership with China’s top drugmaker Hengrui Pharma to develop roughly a dozen new medicines, including four experimental compounds that BMS will send to China for early‑stage clinical testing. Unlike typical licensing deals where U.S. firms outsource Chinese discoveries, this reciprocal arrangement has both companies contributing assets and jointly discovering novel drugs, signaling a shift toward a “global mesh” model of R&D. Industry observers note that American and European biopharma firms are increasingly turning to China for faster, cheaper early‑stage research—potentially cutting development time by half and costs by two‑thirds—while later‑stage trials remain U.S.‑centric to satisfy FDA requirements. The deal underscores China’s growing role as a central hub in global drug development rather than merely a source of one‑off molecules.

Read more: https://www.cnbc.com/2026/05/15/bristol-myers-squibb-turns-to-chinas-hengrui-to-replenish-pipeline.html

#BristolMyers #HengruiPharma #Pfizer #Merck #AstraZeneca #EliLilly #MichaelBaran #McKinsey #DealForma #FDA # #LievenVanderVeken