vovantis
沃提斯实验室 |制药专家
我们为 Vovantis 实验室、制药专家、专业制药、产品专业制药、实验室、临床化学、制造、新型泡腾药物输送系统、医疗药品制造公司、Vovantis 产品、药物研究自有品牌、认证药品制造商、印度古吉拉特邦瓦多达拉拉诺利提供服务
- Type
- Manufacturer
- Location
- India
- Website
- https://vovantis.com
- Categories
- 药品制造, 医疗保健用品
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)