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Czech Republic · APIs

APIs supply to Czech Republic

Zemixal supplies 385 products from its APIs range to buyers in Czech Republic. Demand there comes mainly from generic pharmaceuticals, petrochemicals & refining and automotive components & coatings. Regular consignments go to industrial centres such as Prague, Pardubice and Ústí nad Labem. Typical customers for this division are finished dosage formulators, generic dossier developers and veterinary drug manufacturers.

Czech Republic Sample products
385products in this division
28–36 dsea transit from India
4–6 dair freight
10categories

Supplying APIs to Czech Republic

By sea, containers and LCL lots take roughly 28–36 days to Hamburg (via rail) and Bremerhaven (via rail). Air cargo to Prague (PRG) takes 4–6 days, which suits small and urgent packs. The relevant authority is SÚKL / 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 Czech Republic

AuthoritySÚKL / EMA
SeaportsHamburg (via rail), Bremerhaven (via rail), Koper (via rail)
AirportsPrague (PRG), Ostrava (OSR)
Dangerous goodsIMDG by sea, IATA DGR by air

Czech imports fall under EU REACH and CLP. Registration for substances at 1 tonne or more per year is held by the EU importer or an Only Representative, and SDS and labels must be in Czech. APIs need an EU written confirmation or equivalent GMP standing and must go to a SÚKL-authorised importer. Sea cargo can be cleared at Hamburg or Koper, or moved under transit with a T1 document and cleared at a Czech rail terminal, so agree the clearance point before booking.

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. 28–36 daysOcean transit to Hamburg (via rail)

    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: 35–53 days

By air: about 8–16 days in total.

Documents for Czech Republic

  • 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 Only Representative declaration (substances ≥1 t/yr)
  • SDS in REACH Annex II format in the local language (supplied to the EU importer)
  • EU Written Confirmation for API imports (Art. 46b Directive 2001/83/EC)
  • EORI number of the EU importer (customs declaration)
  • Dangerous Goods Declaration (IMDG/IATA) where applicable
  • T1 transit document where cleared inland

A selection we ship to Czech Republic

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

Full APIs range
Questions

APIs for Czech Republic

Do you ship APIs to Czech Republic?
Yes. We ship by sea to Hamburg (via rail) and Bremerhaven (via rail), 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 Czech Republic?
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 SÚKL / EMA is agreed with you at quote stage.
How long does delivery to Czech Republic take?
Allow 28–36 days for ocean transit or 4–6 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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