Dr. Willmar Schwabe India Pvt.Ltd
Pharmexcil, Hindistan'da kayıtlı büyük ölçekli üretici
Dr. Willmar Schwabe India Pvt.Ltd, Hindistan İlaç İhracatını Teşvik Konseyi (Ticaret ve Sanayi Bakanlığı) Pharmexcil'in üyesidir. Konsey bu şirketi büyük ölçekli bir üretici olarak kaydediyor ki bu bizim çıkarımımız değil, konseyin kendi sınıflandırmasıdır.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- India
- Founded
- 1994
- Website
- https://schwabeindia.com
- Categories
- İlaç Üretimi
- Markets
- Hindistan
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)