HungaroTrial CRO
HungaroTrial - 主页
HungaroTrial 是一个位于中欧和东欧的区域性合同研究组织 (CRO)。自 1999 年以来，我们帮助世界各地的医疗保健组织（包括制药、生物技术和医疗器械公司）推动有效的临床开发。无论您是需要制定确保成功的战略计划、创建稳健的试验流程、了解区域细微差别、加速项目开发，还是有效管理项目整个生命周期的风险，HungaroTrial 都可以为您服务。
- Type
- Manufacturer
- Location
- United Kingdom
- Founded
- 1999
- Website
- https://hungarotrial.com
- Categories
- 药品制造, 医疗保健用品
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)