Accuprec Research Labs Pvt Ltd
USFDA gecontroleerd | NABL- en GLP-gecertificeerd CRO India | Accuprec
USFDA-geauditeerde, NABL- en GLP-gecertificeerde CRO in Ahmedabad. Farmaceutische, medische apparatuur en AYUSH-testen. 1000+ klanten in 60+ landen. IP/BP/USP/ISO-compatibel.
- Type
- Manufacturer
- Location
- Canada
- Website
- https://accuprec.com
- Categories
- Farmaceutische productie, Medische en gezondheidszorgbenodigdheden
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)