Dr. Willmar Schwabe India Pvt.Ltd
Pharmexcil, fabricant enregistré à grande échelle, Inde
Le Dr Willmar Schwabe India Pvt.Ltd est membre de Pharmexcil, le Conseil indien de promotion des exportations de produits pharmaceutiques (ministère du Commerce et de l'Industrie). Le conseil enregistre cette entreprise comme un fabricant à grande échelle, ce qui constitue la propre classification du conseil et non notre déduction.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- India
- Founded
- 1994
- Website
- https://schwabeindia.com
- Categories
- Production pharmaceutique
- Markets
- Inde
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- registry-id-verified (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- registered-since (green), effective since 1994-03-04 Company Master Data (Ministry of Corporate Affairs)
- registered-address (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- cin-on-site (amber), checked 2026-08-11 Published on the company's own website
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- customer-reviews (green), checked 2026-08-09 MouthShut
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
Import rules for these goods
- 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)