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Ireland · Pharmaceutical Intermediates

Pharmaceutical Intermediates for Ireland

Zemixal supplies 14,468 products from its pharmaceutical intermediates range to buyers in Ireland. Locally, the main users are in API & small-molecule manufacturing, biologics and medical devices. Regular consignments go to industrial centres such as Cork (Ringaskiddy / Little Island), Dublin and Limerick – Shannon. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

14,468products in this division
26–35 dsea transit from India
3–5 dair freight
4categories

Supplying pharmaceutical intermediates to Ireland

By sea, containers and LCL lots take roughly 26–35 days to Dublin and Cork. Air cargo to Dublin (DUB) takes 3–5 days, which suits small and urgent packs. The relevant authority is HPRA / EMA. Our export desk lines up the COA, GHS SDS and shipping documents to match. Common grades for this division are Key starting material (KSM) specification, Advanced intermediate (customer spec), Building block, ≥95% / ≥98% purity and Chiral (ee specified).

Grades in this division

Key starting material (KSM) specificationAdvanced intermediate (customer spec)Building block, ≥95% / ≥98% purityChiral (ee specified)Technical gradeLow genotoxic-impurity specification

Pharma compliance in Ireland

AuthorityHPRA / EMA
SeaportsDublin, Cork, Shannon Foynes
AirportsDublin (DUB), Shannon (SNN)
Dangerous goodsIMDG by sea, IATA DGR by air

Ireland applies EU REACH and CLP. Substances imported at 1 tonne or more per year require registration by the EU importer or by an Only Representative for the Indian manufacturer, and SDS and labels must be in English. Active substances for medicines need GMP compliance and an EU written confirmation, and the HPRA supervises authorised importers. Dangerous goods are packed and declared under IMDG or IATA DGR, and customs clearance relies on the importer's EORI number.

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. 26–35 daysOcean transit to Dublin

    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: 33–52 days

By air: about 7–15 days in total.

Documents for Ireland

  • 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 Ireland

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

Full pharmaceutical intermediates range
Questions

Pharmaceutical Intermediates for Ireland

Do you ship pharma intermediates to Ireland?
Yes. We ship by sea to Dublin and Cork, 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 pharma intermediates shipment to Ireland?
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 HPRA / EMA is agreed with you at quote stage.
How long does delivery to Ireland take?
Allow 26–35 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.
Can you scale an intermediate from grams to kilograms without changing the route?
For many listed intermediates the gram packs and the kilogram supply come from the same manufacturing route, which keeps the impurity profile consistent. Where scale-up needs a different route, we tell you before you commit and can provide comparison samples so your team can check the new material against the old.
How do you control isomer and enantiomer content?
Positional isomers are controlled by HPLC or GC methods suited to the compound, and chiral intermediates are tested by chiral HPLC to report enantiomeric excess. The limits that apply to your lot appear on the COA. If your process needs tighter limits, state them on the enquiry and we will confirm what can be met.

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