Dermapharm
医薬品製剤、ジェネリック医薬品、ヘルスケア製品。
Dermapharm は、グルンヴァルト事業所で医薬品製剤、ジェネリック医薬品、ヘルスケア製品を製造しています。同社は、上場主要市場全体の薬局チャネル、病院バイヤー、ヘルスケア流通業者、または輸出顧客に製品を供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Grunwald, Germany
- Founded
- 1991
- Website
- dermapharm.com
- Categories
- 医療およびヘルスケア用品, サプリメントとウェルネス
- Markets
- ドイツ, オーストリア, スイス, フランス
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 ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 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)