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Iceland · APIs

APIs supply to Iceland

The APIs division counts 385 products, and each one can be quoted for delivery to Iceland. In Iceland the strongest demand is from aluminium smelting, geothermal energy & water treatment and fisheries & aquaculture. Regular consignments go to industrial centres such as Reykjavík, Hafnarfjörður (Straumsvík) and Grundartangi. Typical customers for this division are finished dosage formulators, generic dossier developers and veterinary drug manufacturers.

385products in this division
32–45 dsea transit from India
4–7 dair freight
10categories

Supplying APIs to Iceland

By sea, containers and LCL lots take roughly 32–45 days to Reykjavík (Sundahöfn) and Hafnarfjörður. Air cargo to Keflavík (KEF) takes 4–7 days, which suits small and urgent packs. The relevant authority is Icelandic 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 Iceland

AuthorityIcelandic Medicines Agency / EMA
SeaportsReykjavík (Sundahöfn), Hafnarfjörður
AirportsKeflavík (KEF)
Dangerous goodsIMDG by sea, IATA DGR by air

Iceland applies EU REACH and CLP through the EEA Agreement. A substance imported at 1 tonne or more per year must be registered by the importer or by an Only Representative, and SDS and labels are expected in Icelandic. Medicinal active substances follow EEA GMP rules under the Icelandic Medicines Agency. Indian-origin goods that meet the rules can claim India–EFTA TEPA preferences when a valid proof of origin is provided. Dangerous goods must be declared under IMDG or IATA.

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. 32–45 daysOcean transit to Reykjavík (Sundahöfn)

    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 (EEA REACH & CLP) / Environment Agency of Iceland.

Indicative total by sea: 39–62 days

By air: about 8–17 days in total.

Documents for Iceland

  • 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, EEA)
  • Written Confirmation for API imports (EEA application of Directive 2001/83/EC)
  • Dangerous Goods Declaration (IMDG/IATA) where applicable
  • Certificate of Origin supporting India–EFTA TEPA preferences

A selection we ship to Iceland

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

Full APIs range
Questions

APIs for Iceland

Do you ship APIs to Iceland?
Yes. We ship by sea to Reykjavík (Sundahöfn) and Hafnarfjörður, 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 Iceland?
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 Icelandic Medicines Agency / EMA is agreed with you at quote stage.
How long does delivery to Iceland take?
Allow 32–45 days for ocean transit or 4–7 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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