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Denmark · APIs

APIs for Denmark

Buyers in Denmark can order any of the 385 products in our APIs division. Demand there comes mainly from insulin & diabetes care, industrial enzymes & fermentation and biotech & life-science research. Regular consignments go to industrial centres such as Greater Copenhagen / Medicon Valley, Kalundborg and Aarhus. Typical customers for this division are finished dosage formulators, generic dossier developers and veterinary drug manufacturers.

385products in this division
26–34 dsea transit from India
3–5 dair freight
10categories

Supplying APIs to Denmark

By sea, containers and LCL lots take roughly 26–34 days to Aarhus and Copenhagen. Air cargo to Copenhagen (CPH) takes 3–5 days, which suits small and urgent packs. The relevant authority is Danish Medicines Agency / EMA. Our export desk lines up the COA, GHS SDS and shipping documents to match. Common grades for this division are IP, BP, USP and Ph. Eur..

Grades in this division

IPBPUSPPh. Eur.JP (on request)In-house / manufacturer specificationMicronised / particle-size specified

Pharma compliance in Denmark

AuthorityDanish Medicines Agency / EMA
SeaportsAarhus, Copenhagen, Fredericia
AirportsCopenhagen (CPH), Billund (BLL)
Dangerous goodsIMDG by sea, IATA DGR by air

Danish imports fall under EU REACH and CLP. At 1 tonne or more per year, a substance must be registered by the EU importer or by an Only Representative appointed by the Indian maker. Labels and SDS must be in Danish. Active substances for medicines need GMP compliance and an EU written confirmation, and the Danish Medicines Agency supervises authorised importers. Dangerous goods are packed and declared under IMDG or IATA DGR, and the importer's EORI number is needed for customs.

From order to delivery

  1. 1–2 daysQuote and document set agreed

    Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.

  2. 3–7 daysPacking for export

    Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.

  3. 1–3 daysExport clearance at Nhava Sheva or Mundra

    Shipping bill filed, dangerous goods declared under IMDG where needed.

  4. 26–34 daysOcean transit to Aarhus

    Port-to-port time depends on the vessel schedule and any transhipment.

  5. 2–5 daysImport clearance

    Your broker clears the goods against local rules. Chemical oversight: ECHA (EU REACH & CLP).

Indicative total by sea: 33–51 days

By air: about 7–15 days in total.

Documents for Denmark

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • REACH registration number or OR declaration (substances ≥1 t/yr)
  • EU Written Confirmation for API imports (Art. 46b Directive 2001/83/EC)
  • Dangerous Goods Declaration (IMDG/IATA) where applicable
  • Importer's EORI number

A selection we ship to Denmark

A rotating sample from the division. Every product in the catalogue can be quoted for this destination.

Full APIs range
Questions

APIs for Denmark

Do you ship APIs to Denmark?
Yes. We ship by sea to Aarhus and Copenhagen, by air cargo or by express courier depending on quantity and urgency. Every lot carries a COA and a 16-section GHS SDS.
Which documents come with a APIs shipment to Denmark?
Commercial invoice, packing list, certificate of analysis and SDS as standard, plus the bill of lading or air waybill and a certificate of origin. Anything specific to Danish Medicines Agency / EMA is agreed with you at quote stage.
How long does delivery to Denmark take?
Allow 26–34 days for ocean transit or 3–5 days by air, plus packing, export clearance and import clearance. The timeline on this page shows each stage.
What information should I include when requesting an API quotation?
State the molecule, required pharmacopoeia and edition, quantity, intended use and destination country. Mention any special needs such as micronised particle size, a specific polymorph or limits on residual solvents. If your regulator needs manufacturer documents, list them too, so we can confirm availability before pricing.
Can you supply small API samples for formulation trials?
Many APIs can be supplied in development quantities for pre-formulation and stability work. The available sample size depends on the manufacturer and on how the molecule is regulated. Share your project stage and the amount you need, and we will advise what can ship as a sample and what requires a full commercial order.

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