Accuprec Research Labs Pvt Ltd
مدققة من قبل إدارة الغذاء والدواء الأمريكية | NABL & GLP معتمد CRO الهند | أكوبريك
تم تدقيقها من قبل إدارة الغذاء والدواء الأمريكية (USFDA)، وحاصلة على شهادة CRO من NABL وGLP في أحمد آباد. فارما، الأجهزة الطبية واختبار AYUSH. أكثر من 1000 عميل في أكثر من 60 دولة. متوافق مع IP/BP/USP/ISO.
- Type
- Manufacturer
- Location
- Canada
- Website
- https://accuprec.com
- Categories
- تصنيع الأدوية, اللوازم الطبية والرعاية الصحية
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)