Posts in Safety
Rethinking Regulation for Novel Foods

Jurisdictions around the world are actively reviewing how they authorise novel foods. The UK Food Standards Agency (FSA) has a unique opportunity to completely rethink their approach after leaving the EU. A new report considers how their Novel Foods Regulatory Framework could be improved. New concepts such as collaborative regulation and conditional authorisation and supervision could significantly improve the regulatory approval process for foods such as cultured meat and seafood.

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Establishing safety and supporting commercialization for renewable nanomaterials: Vireo at the TAPPI Nanotechnology Conference

Vireo has been working for the past decade to establish safety and support commercialization for microfibrillated cellulose, cellulose nanocrystals and a host of other emerging biomaterials. Our lead scientists are sharing their experience and provide practical guidance in presentations, posters, discussion panels and networking events at the 2023 TAPPI Nanotechnology Conference.

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Cultured meat commercialization and regulatory roundup

Our roundup of the latest cultured meat developments includes announcements from Mosa Meats, Meatable, Aleph Farms, Smart MCs, and UPSIDE, plus commercially-relevant research from Tufts, Kobe University, and Enzymit, FDA approval for consumption of gene-edited pigs, regulatory and governmental perspectives on cultured meat safety research priorities from Vireo and New Harvest, and new labelling requirements in Texas.

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Refreshing nanotechnology environmental, health, and safety research

The U.S. National Nanotechnology Initiative (NNI) is seeking feedback from a broad cross-section of stakeholders as they refresh their Environmental, Health, and Safety (EHS) Research Strategy and reflect on progress toward the goals set in 2011. We encourage individuals, non-governmental organizations, academic and research institutions, and the private sector interested in the responsible development of nanotechnology to join us as we contribute to creating an updated NNI EHS Research Strategy.

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Food safety aspects of cell-based food: A FAO/WHO report

The Food and Agriculture Organization of the United Nations World Health Organization (FAO/WHO) has released a significant new report which identifies potential hazards that could be introduced during production of cultured or cell-based foods and considers the sequence of events that would need to take place for harm to occur to consumers – a critical first step in risk assessment for these new foods.

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FDA to modernize proposed rules defining the identify of foods.

The FDA announced today that they were withdrawing the “Food Standards; General Principles and Food Standards Modernization” rule, proposed in 2005 and were aiming to make FDA definitions and standards of identity for foods consistent with the Federal Food, Drug, and Cosmetic Act, and the standards used by the USDA Food Safety and Inspection Service (FSIS) to inspect meat and poultry products.

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US Cosmetic Law reform provides more oversight powers for FDA and removes requirements for animal testing

The US Congress has passed the first update since 1938 to the federal law regulating personal care products. The FDA will now have some of the same oversight powers for cosmetics that it has for other product categories, and requirements for animal testing on cosmetic products are removed.

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EU Court overturns titanium dioxide carcinogen classification: A salutary tale for toxicity assessment.

In a landmark decision, the EU Court of Justice ruled that 2017 decisions on carcinogenicity for TiO2  did not rely on valid evidence. The animal studies used were not relevant to humans and they failed to show an intrinsic cause of cancer. The court decision has implications for the EU ban of TiO2 in food.

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