vovantis
ヴォバンティス研究所 |製薬スペシャリスト
当社は、Vovantis Laboratories、製薬スペシャリスト、スペシャリストファーマ、製品スペシャリスト製薬、研究室、臨床化学、製造、新規発泡ドラッグデリバリーシステム、医薬品製造会社、Vovantis 製品、医薬品研究プライベートラベル、認定製薬メーカー、インド、ラノリ、バドダラ、グジャラートにサービスを提供しています。
- Type
- Manufacturer
- Location
- India
- Website
- https://vovantis.com
- Categories
- 医薬品製造, 医療およびヘルスケア用品
Verified facts
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- domain-registered (green), checked 2026-08-10 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)