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Jordan · Impurity Reference Standards

Impurity Standards supply to Jordan

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Jordan. Locally, the main users are in generic pharmaceuticals, phosphate & potash fertilisers and cosmetics & detergents. Typical delivery points include Amman, Sahab (King Abdullah II Industrial Estate) and Aqaba. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

20,060products in this division
12–18 dsea transit from India
3–5 dair freight
6categories

Supplying impurity reference standards to Jordan

Sea freight reaches Aqaba in about 12–18 days port to port. Urgent or small lots fly to Queen Alia International, Amman (AMM) in 3–5 days. Import compliance for this category sits with JFDA (Jordan Food & Drug Administration), and we prepare the COA, SDS and commercial documents your broker needs. Common grades for this division are Impurity reference standard with characterisation data, Secondary / working standard, Stable-isotope labelled standard and Nitrosamine (NDSRI) standard.

Grades in this division

Impurity reference standard with characterisation dataSecondary / working standardStable-isotope labelled standardNitrosamine (NDSRI) standardMetabolite standardCustom synthesised impurity

Pharma compliance in Jordan

AuthorityJFDA (Jordan Food & Drug Administration)
SeaportsAqaba
AirportsQueen Alia International, Amman (AMM)
Dangerous goodsIMDG by sea, IATA DGR by air

Hazardous chemicals generally need import approval from the Ministry of Environment, and certain precursors require further clearance from security or drug-control authorities. APIs and excipients fall under the JFDA, which usually expects GMP evidence from the manufacturer and a COA for every batch. Plan for these checks before you place a production-scale order. Most sea cargo enters through Aqaba, so the bill of lading and dangerous goods declaration should name it as the port of discharge. IMDG rules apply at sea and IATA rules for air. There is no India–Jordan trade agreement in force.

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. 12–18 daysOcean transit to Aqaba

    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: Ministry of Environment.

Indicative total by sea: 19–35 days

By air: about 7–15 days in total.

Documents for Jordan

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • Ministry of Environment import approval for hazardous chemicals
  • JFDA import approval for APIs where applicable
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

A selection we ship to Jordan

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

Full impurity reference standards range
Questions

Impurity Reference Standards for Jordan

Can Zemixal deliver impurity reference standards to Jordan?
Yes. We ship by sea to Aqaba, 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 impurity standards shipment to Jordan?
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 JFDA (Jordan Food & Drug Administration) is agreed with you at quote stage.
How long does delivery to Jordan take?
Allow 12–18 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.
How is the purity of an impurity standard determined?
Purity is usually assigned by HPLC area percentage, supported by structural confirmation from NMR and mass spectrometry. Where needed, water content, residual solvents or a mass balance approach are added. The methods used and the results for your lot are listed on the certificate of analysis that comes with the vial.
Can I use your impurity standards in place of official pharmacopoeial references?
Our standards are secondary or research materials, not official pharmacopoeial references. Many laboratories use them for method development, peak identification and routine testing, and keep official references for disputes or regulatory submissions where these are mandated. Your quality system and regulator decide which reference is acceptable for each test.

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