Accuprec Research Labs Pvt Ltd
USFDA Denetlendi | NABL ve GLP Sertifikalı CRO Hindistan | Accuprec
USFDA denetlendi, Ahmedabad'da NABL ve GLP sertifikalı CRO. İlaç, tıbbi cihaz ve AYUSH testi. 60'tan fazla ülkede 1000'den fazla müşteri. IP/BP/USP/ISO uyumlu.
- Type
- Manufacturer
- Location
- Canada
- Website
- https://accuprec.com
- Categories
- İlaç Üretimi, Tıbbi ve Sağlık Malzemeleri
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)