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.
The 14 allergens are celery, cereals with gluten, crustaceans, eggs, fish, lupin, milk, molluscs, mustard, peanuts, sesame, soya, sulphites and tree nuts.
No existe un registro estatal de AAI otorgadas. Cada comunidad publica su listado y MITECO enlaza los 19. Aquí tiene los enlaces y cómo leerlos.
Seit dem 11. März 2026 gibt es keine anzeigepflichtigen Tierseuchen mehr. Die Tierseuchenmeldeverordnung listet alle meldepflichtigen Seuchen.
Avfallsforskriften er Norges hovedforskrift om avfall. Se hva kap 9 om deponi, kap 11 om farlig avfall og kap 13 om eksport av avfall krever.
The Canada DSL is the existing-substance list. An unflagged entry needs no new-substance notice. Check by CAS number, then read an NDSL or blank result.
For a free CAS lookup, paste the number into CAS Common Chemistry, PubChem or EPA CompTox. Use ECHA CHEM for EU status and ECICS for the CN code.
Cyclopentasiloxane (D5) is not banned outright. The EU restricts it at 0.1% or more in wash-off cosmetics, and in leave-on products after 6 June 2027.
EudraLex Volume 4 is the EU GMP guide for human and veterinary medicines. Its four parts, current annexes, 2026 changes and how it differs from US cGMP.
FDA's October 2026 final NDI guidance recommends identity evidence and one safety narrative. The statutory 75-day notification duty has not changed.
ISPM 15 sets debarking, treatment and IPPC stamp rules for wood packaging in trade. The US, EU, UK and Korea can refuse unmarked pallets at import.
Das LFGB ist das deutsche Gesetz für Lebensmittel und Bedarfsgegenstände. Was §§ 30 und 31 verlangen, warum es kein LFGB-Zertifikat gibt und was droht.
Pesticide toxicity classification uses rat LD50: WHO classes Ia to U, GHS Categories 1 to 5, EU CLP Categories 1 to 4 and US EPA Categories I to IV.
化粧品を作って売るには、薬機法の化粧品製造販売業許可（第12条）と製造所ごとの化粧品製造業許可（第13条）があります。申請先は都道府県知事で有効期間は5年。総括製造販売責任者と責任技術者の資格、東京都の手数料、品目ごとの製造販売届、仕入れ販売に許可が要らない条件を条文で確認します。
毒物及び劇物取締法（毒劇法）は、主に急性毒性による健康被害のおそれが高い化学物質を規制する法律です。毒物・劇物・特定毒物の定義、製造・輸入・販売の登録と更新、取扱責任者、医薬用外毒物・劇物の表示色、保管・廃棄、事故届を解説します。登録のない業務上取扱者の義務や施行令、最近の改正も確認できます。
A product monograph is Health Canada's factual, scientific document on a drug's properties, claims and use. See what it contains and how to find one.
REACH-Konformität ist kein Rechtsbegriff. REACH kennt keine Zertifikate. Was Lieferanten nach Art. 31 und 33 schulden und wie sich RoHS unterscheidet.
El registro ICA autoriza vender y usar un plaguicida en Colombia. Cómo consultar si está vigente o cancelado y qué exige la Decisión Andina 804.
The SCOMET declaration format exporters use to confirm goods are off the SCOMET list, when customs asks for it, and how the EUC and licence differ.
EPA's trichloroethylene ban stopped most TCE uses by September 15, 2025. See which products are covered, the later end dates and what EPA has delayed.
WAC pricing is a drug maker's US list price to wholesalers, before discounts and rebates. See how it differs from AWP, ASP, NADAC, AMP and MAC.