Bosnia and Herzegovina · Impurity Reference Standards

Impurity Reference Standards for Bosnia and Herzegovina

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Bosnia and Herzegovina. Locally, the main users are in generic pharmaceuticals, soda ash & coke chemicals and alumina & aluminium. Regular consignments go to industrial centres such as Sarajevo, Tuzla and Lukavac. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Bosnia and Herzegovina Sample products

20,060products in this division

24–32 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Bosnia and Herzegovina

By sea, containers and LCL lots take roughly 24–32 days to Ploče (Croatia, via road/rail) and Split (Croatia, via road). Air cargo to Sarajevo (SJJ) takes 4–7 days, which suits small and urgent packs. The relevant authority is ALMBIH (Agency for Medicinal Products and Medical Devices of Bosnia and Herzegovina). Our export desk lines up the COA, GHS SDS and shipping documents to match. 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 Bosnia and Herzegovina

Authority	ALMBIH (Agency for Medicinal Products and Medical Devices of Bosnia and Herzegovina)
Seaports	Ploče (Croatia, via road/rail), Split (Croatia, via road), Rijeka (Croatia, via rail)
Airports	Sarajevo (SJJ), Tuzla (TZL)
Dangerous goods	IMDG by sea, IATA DGR by air

Chemicals regulation in Bosnia and Herzegovina is split between the Federation of BiH and Republika Srpska, and both are moving toward REACH and CLP. Importers should confirm registration and labelling rules with the relevant entity authority and prepare a local-language SDS. Medicines and APIs are regulated at state level by ALMBIH in Banja Luka, which expects GMP evidence. Precursors need import permits. Sea cargo is usually cleared after transit from Ploče in Croatia, and dangerous goods follow IMDG or IATA.

From order to delivery

1–2 daysQuote and document set agreed
Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.
3–7 daysPacking for export
Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.
1–3 daysExport clearance at Nhava Sheva or Mundra
Shipping bill filed, dangerous goods declared under IMDG where needed.
24–32 daysOcean transit to Ploče (Croatia, via road/rail)
Port-to-port time depends on the vessel schedule and any transhipment.
2–5 daysImport clearance
Your broker clears the goods against local rules. Chemical oversight: Entity-level chemicals laws (Federation of BiH and Republika Srpska), progressively aligned with EU REACH/CLP.

Indicative total by sea: 31–49 days

By air: about 8–17 days in total.

Documents for Bosnia and Herzegovina

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Local-language SDS (prepared by the importer)
GMP certificate / manufacturer authorisation for APIs
Import permit for precursor or controlled chemicals where applicable
Dangerous Goods Declaration (IMDG/IATA) where applicable

Categories in impurity reference standards

API Impurities 9,055Pharmacopeial Impurities (EP / USP / BP) 3,890Nitrosamine Impurities 382Stable Isotope Labelled Standards (Deuterated, 13C, 15N) 976Metabolites & Degradation Products 2,569API Reference Standards 3,188

A selection we ship to Bosnia and Herzegovina

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

Full impurity reference standards range

Vadadustat Methyl Acetate Impurity

CAS: 1000024-87-2
Formula: C₁₅H₁₃ClN₂O₄
MW: 320.73 g/mol

ZX-027489

Valaciclovir EP Impurity C Hydrochloride

CAS: 1346617-39-7
Formula: C₁₄H₂₃ClN₆O₄
MW: 374.82 g/mol

ZX-027490

Valaciclovir EP Impurity R

CAS: 142963-60-8
Formula: C₁₃H₂₀N₆O₄
MW: 324.34 g/mol

ZX-027491

Valaciclovir EP Impurity M

CAS: 847670-62-6
Formula: C₁₄H₂₀N₆O₅
MW: 352.35 g/mol

ZX-027492

Valaciclovir EP Impurity F

CAS: 86150-61-0
Formula: C₁₄H₂₃NO₆S
MW: 333.4 g/mol

ZX-027493

Valaciclovir EP Impurity P

CAS: 1356019-51-6
Formula: C₂₇H₄₀N₁₂O₈
MW: 660.7 g/mol

ZX-027494

Valganciclovir O-Acetyl N-Benzyloxycarbonyl Impurity

CAS: 194159-22-3
Formula: C₂₄H₃₀N₆O₈
MW: 530.5 g/mol

ZX-027495

Valganciclovir EP Impurity R

CAS: 1654737-32-2
Formula: C₁₄H₂₁ClN₆O₄
MW: 372.81 g/mol

ZX-027496

Valganciclovir EP Impurity O

CAS: 119089-68-8
Formula: C₁₆H₁₉N₅O₄
MW: 345.35 g/mol

ZX-027497

Valganciclovir Homolog(component G as per USP)

CAS: 1356932-88-1
Formula: C₁₅H₂₄N₆O₆
MW: 384.39 g/mol

ZX-027498

(+/-)-2-Propyl-4-pentenoic Acid

CAS: 1575-72-0
Formula: C₈H₁₄O₂
MW: 142.2 g/mol

ZX-027499

Valsartan Methyl Ester

CAS: 137863-17-3
Formula: C₂₅H₃₁N₅O₃
MW: 449.5 g/mol

ZX-027500

Questions

Impurity Reference Standards for Bosnia and Herzegovina

Do you ship impurity standards to Bosnia and Herzegovina?

Yes. We ship by sea to Ploče (Croatia, via road/rail) and Split (Croatia, via road), 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 Bosnia and Herzegovina?

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 ALMBIH (Agency for Medicinal Products and Medical Devices of Bosnia and Herzegovina) is agreed with you at quote stage.

How long does delivery to Bosnia and Herzegovina take?

Allow 24–32 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.

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.

Other divisions for Bosnia and Herzegovina

Lab Reagents Solvents (HPLC & GC) Biochemicals APIs Pharmaceutical Intermediates Inorganics & Metals Specialty Chemicals

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