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.
诺德马克制药有限公司
生物制药活性成分和药物的全面解决方案合作伙伴我们塑造健康的未来。生物技术：我们对未来医学的贡献！了解更多 我们塑造健康的未来。可靠的患者护理 - 德国制造 了解更多 公司数据、数据和事实 生物技术 我们对未来医学的贡献 生物化学品 用于研究和临床的生物化学品 职业生涯 立即在 Nordmark 开始 Nordmark - 来自单一来源的完整解决方案 Nordmark 专门生产生物和生物技术来源的活性成分和药物。通过将我们的活动集中在制药行业的这个利基市场，我们成功地将自己定位于国际市场。尤其是在Pankr的制作中
- 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
- 药品制造, 化学品与塑料, 补充剂与健康
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 在这里，中标还附带了别人做过的审查：在欧盟和欧洲经济区，公共采购方必须排除因欺诈、腐败或洗钱被定罪的投标人，以及经终局裁决认定拖欠税款或社会保险费的投标人。 这项审查只针对那次招标、截至授标之日：它不说明公司今天的状况，中标也不说明合同已经履行。 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: 药品制造 (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 化学品与塑料, 补充剂与健康: 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.