Peer review of the pesticide risk assessment of the active substance fatty acids from hydrolysed vegetable oils
EFSA Journal, Volume 24, Issue 11, November 2026.
Weekly collection from GOV.UK, legislation.gov.uk, EUR-Lex, CJEU, EFSA and the US Federal Register (last run 12 Nov 2026), plus a curated register with business impact, actions and deadlines.
Register + feed · click to filter
Established → Evolving → Emerging
Established = binding / final. Evolving = proposal or consultation. Emerging = early signal or scientific assessment.
Loading…
14 items.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
EFSA Journal, Volume 24, Issue 11, November 2026.
Results from the UK government’s monitoring of pesticide residues in food grown in the UK and in imported food.
The Food and Drug Administration (FDA, the Agency, or we) is announcing the availability of a draft guidance for industry entitled "Action Levels for Cadmium in Processed Food Intended for Babies and Young Children." The draft guidance, when finalized, will establish action levels for cadmium in certain processed foods intended for babies and young children less than 2 years old. The draft guidance is intended to set achievable action levels that will help further reduce cadmium in the food supply.
Risk assessment of dietary cadmium exposure during pregnancy, supporting food safety advice on potential risks to maternal and offspring health.
The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry titled "Regulatory Considerations for Prescription Drug Use-Related Software." This final guidance describes FDA's application of its drug labeling authorities to certain software outputs that are disseminated by or on behalf of a drug sponsor for use with a prescription drug product or a prescription drug-led, drug-device combination product that is assigned to the Center for Drug Evaluation and Research or the Center for Biologics Evaluation and Research as the lead center. This guidance finalizes the draft guidance of the same title issued on September 19, 2023.
The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection provisions of FDA's guidance for industry entitled "Channels of Trade Policy for Commodities With Residues of Pesticide Chemicals, for Which Tolerances Have Been Revoked, Suspended, or Modified by the Environmental Protection Agency Pursuant to Dietary Risk Considerations."
Annual summary of the work carried out by the UK Expert Committee on Pesticides (ECP).