Dr. Willmar Schwabe India Pvt.Ltd
Pharmexcil зарегистрировал крупного производителя в Индии.
Доктор Уиллмар Швабе India Pvt.Ltd является членом Pharmexcil, Совета по содействию экспорту фармацевтических препаратов Индии (Министерство торговли и промышленности). Совет регистрирует эту компанию как крупного производителя, что является собственной классификацией совета, а не нашим выводом.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- India
- Founded
- 1994
- Website
- https://schwabeindia.com
- Categories
- Фармацевтическое производство
- Markets
- Индия
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)