Our Scans
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Food & Drug Administration
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Weekly Summary
[New] Regulatory Compliance and Recall Risk: The US FDA and AAFCO impose stringent nutritional standards and ingredient labeling requirements.
IMARC Group
[New] The FDA recently released a warning letter alerting life science orgs to the risks of using and advising against overreliance on AI in drug manufacturing.
Forrester
[New] The $50 million federal matching fund and the mandated data-sharing agreements between HHS, the FDA, and the VA are expected to significantly increase both the volume and quality of clinical evidence supporting psychedelic therapies.
Keta Medical Center
[New] FDA-approved TDXd toxicity: proactive multiday antiemetic management; CT ILD screening every third cycle; hard stop at grade 2; renal insufficiency is an underrecognized risk factor.
The Cancer News
[New] Revolution Medicines plans to submit a new drug application to the FDA and intends to benefit from the FDA Commissioner's National Priority Voucher pilot programme, which is designed to accelerate review of therapies aligned with US national health priorities.
Life Science Daily News
[New] FDA clearance of Sibel Health's wireless maternal-foetal monitoring platform will increase competitive pressure on established manufacturers to accelerate R&D of wireless alternatives to traditional wired cardiotocography systems.
Fitch Solutions
[New] The US FDA this week recommended that people use serial testing-taking multiple COVID-19 tests over several days - to reduce the risk of a false-negative result and to help prevent people from unknowingly spreading the SARS-CoV-2 virus to others.
The Council of Industry
[New] Since cultivated meat is jointly regulated by USDA-FSIS and FDA, every cultivated meat producer will need to register its facilities with FDA (regardless of the type of product they make). / USA
The Good Food Institute
Last updated: 19 June 2026
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