Statens Serum Institut
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.
Statens Serum Institut (SSI) is a research institution under the Ministry of Health in Denmark, dedicated to preventing and combating infectious diseases and congenital disorders…
Statens Serum Institut (SSI) adalah lembaga penelitian di bawah Kementerian Kesehatan di Denmark, yang didedikasikan untuk mencegah dan memerangi penyakit menular dan kelainan bawaan…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Denmark
- Website
- http://ssi.dk
- Categories
- Manufaktur Farmasi
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 8 official records from 8 official sources are on file. 1 other entry is not an official record: 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
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 1996. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-02. Internet Archive (Wayback)
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. checked 2026-09-07. GLEIF global LEI register (golden copy)
- registry-activity (record type: registry-activity) [official record; status green] Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-09-23. Lægemiddelstyrelsen, virksomheder med tilladelse efter § 39 stk. 1
- Takes part in public tenders (record type: public-contract-awarded) [official record; status green] 4 public contracts on record, the latest awarded 2026-03-03. A public buyer selected this supplier through an official tender. Open the source for the contracts themselves. effective since 2026-03-03. TED (Tenders Electronic Daily), EU public procurement award notices Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. Pemeriksaan itu berlaku untuk tender tersebut pada tanggal penetapan pemenang: tidak menunjukkan keadaan perusahaan saat ini, dan menang tender tidak menunjukkan bahwa kontraknya telah dilaksanakan. 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 2025-08-27. EudraGMDP, EU register of GMP certificates (EMA)
- 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)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-08-21. Jordan Food and Drug Administration (JFDA), approved manufacturing sites (open data portal of Jordan)
- 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
Import rules for these goods
Product-specific import rules not established for the catalog category Manufaktur Farmasi: neither the company's own description nor an official activity code shows that its own goods are of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.