Dermapharm
Formulações farmacêuticas, medicamentos genéricos e produtos de saúde.
A Dermapharm fabrica formulações farmacêuticas, medicamentos genéricos e produtos de saúde a partir de suas operações em Grunwald. A empresa fornece canais farmacêuticos, compradores de hospitais, distribuidores de serviços de saúde ou clientes de exportação em seus principais mercados listados.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Grunwald, Germany
- Founded
- 1991
- Website
- dermapharm.com
- Categories
- Suprimentos médicos e de saúde, Suplementos e bem-estar
- Markets
- Alemanha, Áustria, Suíça, França
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 2026-08-02 Domain registry record
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- public-contract-awarded (green), effective since 2026-07-02 TED (Tenders Electronic Daily), EU public procurement award notices Aqui a adjudicação traz também uma verificação feita por outros: na UE e no EEE o comprador público tem de excluir concorrentes condenados por fraude, corrupção ou branqueamento, e aqueles com dívidas fiscais ou contributivas fixadas por decisão definitiva. Directive 2014/24/EU, Article 57 (exclusion grounds)
- vat-valid (green), checked 2026-08-18 VIES (European Commission)
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)