ciron drugs+ pharmaceuticals pvt ltd
Hersteller pharmazeutischer Formulierungen in Indien - Pharmaexporteure in Mumbai - CIRON Group, Mumba
Die Ciron Group ist einer der führenden Hersteller pharmazeutischer Formulierungen in Indien. Ciron gehört auch zu den führenden Exporteuren pharmazeutischer Formulierungen in Mumbai. Eine fortschrittliche Pharmamarke, die sich für das Wohl der Menschheit einsetzt.
- Type
- brand seeking distribution
- Location
- Mumbai, India
- Website
- https://www.cironpharma.com
- Categories
- Pharmazeutische Produktion, Verpackungs- & Druckbedarf, Industriemaschinen
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- customer-reviews (green), checked 2026-08-08 MouthShut
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registered-trade-only (amber), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
Import rules for these goods
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
- 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)