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Bagged, Precut Onions Tied to Salmonella Illnesses in 22 States

Drugs.com

25, 2023 – Federal regulators are investigating a salmonella outbreak linked to packaged, diced onions that has sickened at least 73 people across 22 states. WEDNESDAY, Oct. Fifteen of the illnesses were so bad that people required.

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Product Highlight: DrugBank on Snowflake Marketplace

DrugBank

That’s why DrugBank is making it easier than ever to access our data packages through Snowflake Marketplace, allowing you to explore and trial our offerings seamlessly to support your work and enhance decision-making.

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How GPCR-targeting therapies are advancing the fight against inflammatory disease

Drug Target Review

All these features make GPCRs central to regulating many vital biological processes in the body, including immune responses and inflammation, and thus especially attractive for therapeutic intervention. Meet the author Stephan Schann is Chief Scientific Officer at Domain Therapeutics.

Disease 59
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Understanding the Elements of a Typical IND-Enabling Package

The Premier Consulting Blog

While the type, number, and design of these studies vary based on product-specific characteristics, IND-enabling packages submitted to the FDA generally include key information about the pharmacology, pharmacokinetics, and toxicology of the product. Primary pharmacology examines the on-target effects on the drug such as receptor binding.

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Companies Shipping Chemicals: “Know the One You’re Dancing With”

FDA Law Blog: Biosimilars

DEA seized five packages in Eagle Pass, Texas, identifying IMC Pro as the shipper containing 26.4 1-BOC-Piperidone is a DEA-regulated List 1 chemical while (2-Bromethyl) benzene is on DEAs longstanding, recently updated Special Surveillance List. IMC Pro did not store or handle the packages nor maintain records about their contents.

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The Role of Quality Assurance in Generic Drugs

Drug Patent Watch

Quality Assurance is a team effort : From manufacturers to regulators, QA professionals, and beyond, everyone plays a critical role in ensuring the quality and safety of generic drugs. So, I ask you: What do you think is the most important aspect of Quality Assurance in the generic drug industry?

Drugs 77
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Commission unveils “one substance, one assessment” reform package

Agency IQ

With the publication of three proposed legal acts, this concept is one step closer to streamlining the way the bloc regulates chemicals. The Commission has long aspired to realize its one substance, one assessment concept in the EU’s chemical regulatory regime. Fill out the form to read the full article.