Nordmark Pharma GmbH
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
ノードマーク ファーマ GmbH
バイオ医薬品の有効成分と医薬品のフルソリューションパートナー 私たちは健康な未来を形作ります。バイオテクノロジー：未来の医療への貢献！詳細はこちら 私たちは健全な未来を形作ります。信頼性の高い患者ケア - ドイツ製 詳細はこちら 会社概要、データ、事実 バイオテクノロジー 未来の医療への貢献 生化学 研究およびクリニック向け生化学 キャリア 今すぐ Nordmark で始めましょう Nordmark - 単一ソースからの完全なソリューション Nordmark は、生物学的およびバイオテクノロジー起源の有効成分および医薬品の生産を専門としています。製薬業界のこのニッチ市場に活動を集中させることで、当社は国際的に地位を確立することに成功しました。特にパンクルの制作においては
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Uetersen, Germany
- Website
- https://www.nordmark-pharma.de
- Categories
- 医薬品製造, 化学薬品とプラスチック, サプリメントとウェルネス
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 9 official records from 9 official sources are on file. 2 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-08-22. VIES (European Commission)
- Site address listed in a government regulator's register (record type: facility-registered) [official record; status green] Shows the regulator records a site of this company at a named address. A registration is not an observation of current production. effective since 2022-06-13. Industrieanlagen nach EU-Industrieemissionsrichtlinie, Schleswig-Holstein (LIS-A)
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. checked 2026-08-15. OpenSanctions
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. checked 2026-08-15. OpenSanctions
- Active legal entity ID (LEI) (record type: lei-active) [official record; status green] A global identifier used in finance; an active one is renewed yearly. checked 2026-09-07. GLEIF global LEI register (golden copy)
- Takes part in public tenders (record type: public-contract-awarded) [official record; status green] 7 public contracts on record, the latest awarded 2026-07-31. A public buyer selected this supplier through an official tender. Open the source for the contracts themselves. effective since 2026-07-31. 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。 この審査はその入札の落札日時点のものです。会社の現在の状況を示すものではなく、落札は契約が履行されたことを示すものでもありません。 Directive 2014/24/EU, Article 57 (exclusion grounds)
- Market access approved: European Union (record type: market-access-eu) [official record; status green] Shows the establishment is approved for the listed activities under the EU food-hygiene rules and appears in the EU list of approved establishments. It is not an import check and not an observation of current production. checked 2026-08-22. TRACES NT, European Commission register of approved establishments (DG SANTE)
- GMP certificate from a medicines agency (record type: gmp-certified) [official record; status green] A medicines regulator inspected the site and confirmed it may manufacture medicines. effective since 2025-07-10. EudraGMDP, EU register of GMP certificates (EMA)
- Holds a registered role on the national energy market (record type: energy-market-role-operator) [official record; status green] Shows the company is registered in the national energy-market register as the operator of 1 energy installations at its own sites. Operating such an installation does not make energy its main business. checked 2026-08-17. Marktstammdatenregister (Bundesnetzagentur)
- Medicines manufacturing or import authorisation (MIA) (record type: medicines-mia-holder) [official record; status green] A medicines regulator authorises this company to manufacture and/or import medicinal products at the named site. The register lists the authorisation itself, not which products it covers, and it is not a record of trading. checked 2026-08-15. EudraGMDP manufacturing and importation authorisation register (EMA)
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-10. GLEIF Global LEI record
Relationships
4 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Recorded in a source
- Pinnauallee 4, 25436, Uetersen: Holds the site's permit, registry number DE01056000133. TRACES NT, European Commission register of approved establishments (DG SANTE)
- Uetersen: Manufactures at the site. EudraGMDP, EU register of GMP certificates (EMA)
Candidates, not confirmed
- Germany: Site named by the company itself, not confirmed by a record, country DE. nordmark-pharma.de
- nordmark-pharma.de: Website of this business. Source record
Profiles
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)
Goods family established: 医薬品製造 (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog categories 化学薬品とプラスチック, サプリメントとウェルネス: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.