Regulatory questions, answered.
Questions asked in RegAffairs AI and answered from official sources, with every claim cited to the document it came from.
Which rodenticides are registered in Canada?
Health Canada's PMRA register currently lists 182 product registrations whose product type includes "rodenticide", built on 19 active ingredients.
Hvilke virksomheter må ha bedriftshelsetjeneste?
Virksomheter må ha bedriftshelsetjeneste på to grunnlag etter § 13-1 i forskrift om organisering, ledelse og medvirkning (FOR-2011-12-06-1355): (1) alle…
Which solvents are VOC exempt in California?
California has no single list of exempt solvents. Which list applies depends on the rule that covers your product.
How should chlorine disinfectants be used on workplace surfaces?
Use chlorine disinfectants only where disinfection is actually needed.
How do I check whether a pesticide is registered in California?
Use the California Department of Pesticide Regulation (DPR) product registration records.
Tıbbi cihaz nedir?
Türkiye'de tıbbi cihazın yasal tanımı Tıbbi Cihaz Yönetmeliği Madde 3(1)(eee) bendinde yer alır.
What is TSCA certification for imports?
TSCA import certification is a statement the importer of record (or its authorised agent) files with US Customs and Border Protection (CBP) before release of…
KOSHA MSDS에서 CAS 번호로 물질을 어떻게 찾나요?
CAS 번호를 하이픈까지 포함한 전체 형식(예: 71-43-2)으로 알려 주시면, 그 번호와 정확히 일치하는 KOSHA 참조 MSDS를 바로 찾아 드립니다.
GLP 뜻이 뭔가요?
GLP는 Good Laboratory Practice(우수실험실운영기준)의 약자입니다. 비임상(non-clinical) 시험을 대상으로 하는 품질보증 시스템으로, 사람의 건강과 환경에 관한 안전성 시험을 어떤 조직과 조건에서 계획하고 수행하고 감독하는지, 그리고 그 결과를 어떻게…
Os neonicotinoides são proibidos no Brasil?
Não. Os neonicotinoides não são proibidos no Brasil. As monografias da ANVISA dão como autorizados o imidacloprido (I13), o tiametoxam (T48), a clotianidina…
Como consultar o registro de um medicamento na Anvisa?
Para consultar o registro de um medicamento na Anvisa, use o serviço gratuito Consulta a Registro de Medicamentos no portal gov.br.
医療機器の回収情報はどこで確認できますか？
日本の医療機器の回収情報は、PMDA（独立行政法人 医薬品医療機器総合機構）のウェブサイトの「回収情報（医療機器）」で確認できます。年度別・クラス別（クラスI〜III）の一覧があり、そこから回収番号ごとの回収概要ページを開く構成です。回収の報告義務は医薬品医療機器等法 第六十八条の十一に定められています。
What is a DIN number in Canada?
A DIN (Drug Identification Number) is the number Health Canada assigns to a drug product before it can be sold in Canada.
¿Qué exige México para remediar suelos contaminados con hidrocarburos?
México exige que el responsable de la contaminación remedie todo suelo en el que los hidrocarburos superen los límites máximos permisibles de la…
What are the ICH stability guidelines?
The ICH stability guidelines are the Q1 series (Q1A(R2) to Q1E) plus Q5C for biotechnological/biological products.
Where can I find Australia's food additives list?
Australia's food additives list is part of the Australia New Zealand Food Standards Code, which Food Standards Australia New Zealand (FSANZ) maintains.
What is the CLP regulation?
The CLP Regulation is Regulation (EC) No 1272/2008 on the classification, labelling and packaging of substances and mixtures.
Wanneer heb ik een begeleidingsbrief voor afvalstoffen nodig?
In Nederland heb je een begeleidingsbrief nodig bij elk transport van afvalstoffen.
Welche Pflichten gelten nach dem Schweizer Produktesicherheitsgesetz?
Wer in der Schweiz gewerblich oder beruflich Produkte in Verkehr bringt, muss nach dem Produktesicherheitsgesetz (PrSG, SR 930.11) vier Dinge leisten: Das…
What is an in vitro diagnostic medical device?
In EU law, an in vitro diagnostic medical device (IVD) is a medical device used outside the body ("in vitro") to examine specimens taken from the human body…