Accuprec Research Labs Pvt Ltd
美国FDA审核|印度 CRO 获得 NABL 和 GLP 认证 |埃库普雷克
位于艾哈迈达巴德的经美国 FDA 审核、NABL 和 GLP 认证的 CRO。制药、医疗器械和 AYUSH 测试。 60 多个国家/地区的 1000 多个客户。符合 IP/BP/USP/ISO 标准。
- Type
- Manufacturer
- Location
- Canada
- Website
- https://accuprec.com
- Categories
- 药品制造, 医疗保健用品
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- domain-registered (green), checked 2026-08-03 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)