机构信息

监管背景

确认订单前,请核对预期用途、材料类别和目的地。

审阅要点

研究材料、活性成分和获批药品是不同类别。研究用途标签不能替代采购、进口、操作或使用所适用的要求。

准备咨询

请提供产品或序列、配置、数量、目的地和所需文档,以便团队评估范围并确认可提供的信息。

来源与核实范围

官方/监管来源 · S12

Anvisa orienta sobre importação de insumos para canetas de GLP-1 ↗

ANVISA

来源详情(原文语言)
范围
Historical guidance on GLP-1 active ingredients
文件位置
Identification and commercial import sections
局限
Must be read with later updates; does not establish eligibility of RUO catalog products.
陈述核实日期
2026-09-09
官方/监管来源 · S13

Novas medidas sobre importação e manipulação de GLP-1 ↗

ANVISA

来源详情(原文语言)
范围
Announcement of inspection and review measures
文件位置
Inspection and proposed regulatory review measures
局限
Announcement is not a blanket authorization or a complete consolidated legal rule.
陈述核实日期
2026-09-09
官方/监管来源 · R02

Importing Biological Materials into the United States ↗

U.S. Customs and Border Protection

来源详情(原文语言)
范围
US import requirements depend on material and applicable agencies
文件位置
Agency requirements and scope
局限
Research use does not automatically remove applicable requirements; no universal catalog admission claim.
陈述核实日期
2026-09-09
官方/监管来源 · R01

FDA approves new medication for chronic weight management ↗

FDA

来源详情(原文语言)
范围
US approval of Zepbound (tirzepatide) for the stated adult indication
文件位置
Zepbound approval announcement
局限
Approval applies to that medicinal product and jurisdiction, not research vials.
陈述核实日期
2026-09-09