Notes on doing the research.
Industry-neutral writing about the work itself: how to cite a paragraph, when to stop, and what a trail is for. Not product announcements.
BPA receipts face a 0.02% limit in the EU and GB from 2 January 2020. BPS replaced much of that paper, and BPA-free is not the same as phenol-free.
Learn when Victoria requires an environmental audit, who can conduct it, how a preliminary risk screen works and what the audit statement means.
FD&C colors are synthetic food dyes that FDA lists in 21 CFR Part 74 and certifies batch by batch. Seven are allowed in US food. Red No. 3 ends in 2027.
Die GESTIS-Stoffdatenbank des IFA ist kostenlos und hat Datenblätter zu rund 8.800 Reinstoffen. So suchen Sie nach Name oder CAS und lesen ein Datenblatt.
Glyfosaat is niet volledig verboden in Nederland. De EU-goedkeuring loopt tot 2033. Lees wat geldt voor landbouw, particulieren en ander gebruik.
Miljøgifter brytes ned sakte og kan hope seg opp og gi langtidsskader. Se norske eksempler, prioritetslista, forbud og regler om varsling ved eksport.
Nanotechnology in cosmetics means nano ingredients such as zinc oxide in sunscreen. Compare EU and GB labelling and notification rules with the US safety requirements.
The US R22 phase out ended HCFC-22 production and import in 2020. Existing systems can still be serviced. India allows limited servicing until 2040.
Waste tracking in Australia: how each state tracks hazardous waste, what J120 and N120 mean, Queensland certificates and NEPM interstate rules.
Kunststof bamboe servies met bamboevezel mag niet worden verkocht in de EU. Lees welke regels gelden voor echt bamboe en melamine en wat de NVWA vond.
トルエンは毒物及び劇物取締法の劇物です。指定令第2条第1項第七十六号の二は原体のみを指定し、含有製剤や濃度除外の規定はありません。混合物は他の成分の指定も確認します。メタノール、キシレン、アセトニトリル、苛性ソーダなどの該当号と濃度基準、劇物表示やSDSに関わる主な注意点を説明します。
China food safety standards are mandatory GB standards from the NHC and SAMR. Imports must meet them. Labelling standards apply from March 2027.
Corantes alimentares são aditivos que dão cor ao alimento. Veja a lista da Anvisa (IN 211/2023), a regra do rótulo e a IDA dos principais corantes.
E-Phy est le catalogue ANSES des produits phyto autorisés en France. Cherchez par nom ou n° d'AMM pour voir doses, DAR, ZNT et dates de retrait.
La icaridina es un repelente aprobado en la UE hasta 2032. Qué concentración usar, desde qué edad, en el embarazo y frente a DEET, IR3535 y citriodiol.
La malattia professionale è un'infermità contratta a causa del rischio delle lavorazioni. Definizione INAIL, tabelle 2023 e differenza con l'infortunio.
UK skin lightening creams must meet cosmetics rules. Hydroquinone, mercury and steroids are banned in skin creams. Check importer and seller duties.
The use dilution test checks liquid disinfectants on 60 steel carriers. Hospital claims pass at no more than 3/60 and 6/60 positive carriers.
ヒヤリハットとは、けがや病気に至らなかった危険な出来事です。意味と語源、英語表現、ハインリッヒの法則（1:29:300）、インシデントや労働災害との違いを解説。報告・共有から改善につなげる活動の目的と進め方、職場のあんぜんサイトの事例の探し方を、厚生労働省と労働局の公的資料で確認できます。
Il D.Lgs. 81/08 è il Testo unico sicurezza sul lavoro del 9 aprile 2008: struttura, obblighi di datore e lavoratori, modifiche 2024-2026, testo vigente.
The EU Pesticides Database is the Commission's free tool for active substance approvals, MRLs and emergency authorisations. Here is how to read it.
Choose a food testing lab in India by checking its accreditation scope, FSSAI status, six-monthly testing duties and the limits used in its report.
Le glyphosate reste autorisé en France pour les professionnels, avec 10 produits et des doses plafonnées. Il est interdit aux particuliers depuis 2019.
GMP in Canada is law: Part C, Division 2 of the Food and Drug Regulations. How GUI-0001, Health Canada inspections and FDA cGMP fit together.
NPRI data lists each Canadian facility's pollutant releases, disposals and transfers since 1993. Search it online, map it or download the open data files.
La scheda di sicurezza (SDS) ha 16 sezioni fissate dal REACH e dal reg. 2020/878. Chi deve fornirla, quando aggiornarla, come leggerla e dove trovarla.
Canada listed BPA as toxic under CEPA in 2010. Polycarbonate baby bottles and cosmetics are prohibited. Food cans and thermal receipts are not.
El etiquetado textil en España sigue el Reglamento (UE) 1007/2011 y el Real Decreto 928/1987. Nombres de fibra, porcentajes, tolerancias e idioma.
A food hygiene rating scores businesses from 0 to 5 in England, Wales and Northern Ireland. Learn what each score means and how inspectors set it.
Phthalates in cosmetics face listed bans in the EU and GB, a class ban in Washington and a DBP and DEHP ban in California. US federal law bans none.
RIDDOR stands for the Reporting of Injuries, Diseases and Dangerous Occurrences Regulations 2013, the GB law on reporting serious work incidents to HSE.
The SCIP database is ECHA's register of articles holding Candidate List SVHCs above 0.1% w/w. Who must notify, what to submit, and the repeal status.
Glyphosate in food is legal up to crop MRLs and shows up most in wheat, oats, barley and soybeans. ADIs differ: EU 0.5, Codex 0-1, EPA chronic RfD 1.0.
Hexabromocyclododecane (HBCDD) is a brominated flame retardant once used in polystyrene insulation. The EU trace limit is 75 mg/kg. China bans it.
The current Humira package insert is FDA supplement S-425, Revised 12/2025, on Drugs@FDA (BLA 125057) and DailyMed. Where to get it and what it contains.
Natasha's Law requires UK food prepacked for direct sale to carry its name and a full ingredients list with the 14 allergens emphasised, from 1 Oct 2021.
A controlled substance schedule is one of five US categories (I to V) set by the Controlled Substances Act. The binding list is 21 CFR Part 1308.
Environmental clearance (EC) is prior approval under the EIA Notification 2006 for listed projects. See Category A vs B, the process, documents and SEIAA.
CosIng is the European Commission's free database of cosmetic ingredients, INCI names and Annex entries. How to search it and what it can't tell you.
A short checklist for reading a cited regulatory answer under time pressure, whether it came from a colleague, a consultant or a research agent.
Retainers are for judgement. Status checks, scope questions and cross-market deltas should not wait for a kickoff call. How to split the work.
Most of the binding detail in a modern instrument lives in a table. A short method for not missing the row that actually applies.
The most expensive regulatory answers are the ones that fill a gap with a plausible sentence. How to treat silence as a finding.
Cross-market regulatory questions fail when they are answered as eight separate memos. How to ask for the differences that actually change the work.
An answer without a method is a claim. Why the steps behind a regulatory answer belong on the same page as the sentence you will quote.
A regulatory answer you cannot re-find is not an answer. How to pin a claim to the instrument, annex and paragraph someone else can open.