Georgia · Impurity Reference Standards

Impurity Reference Standards for Georgia

Buyers in Georgia can order any of the 20,060 products in our impurity reference standards division. In Georgia the strongest demand is from generic pharmaceuticals, mining & ferroalloys and wine & food processing. Typical delivery points include Tbilisi, Rustavi and Kutaisi. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Georgia Sample products

20,060products in this division

30–42 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Georgia

Sea freight reaches Poti and Batumi in about 30–42 days port to port. Urgent or small lots fly to Tbilisi (TBS) in 3–6 days. Import compliance for this category sits with Regulation Agency for Medical and Pharmaceutical Activities (Ministry of Health), 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 Georgia

Authority	Regulation Agency for Medical and Pharmaceutical Activities (Ministry of Health)
Seaports	Poti, Batumi, Anaklia (under development)
Airports	Tbilisi (TBS), Kutaisi (KUT)
Dangerous goods	IMDG by sea, IATA DGR by air

Georgia's customs regime is relatively straightforward. Under its EU Association Agreement, the country is phasing in CLP-style classification and labelling, so GHS-format SDS are well accepted. Georgian-language labelling may be required for some products. Pharmaceutical substances are overseen by the Regulation Agency for Medical and Pharmaceutical Activities, and controlled precursors or narcotics need permits. Cargo consigned onward from Poti or Batumi to neighbouring countries needs a transit declaration. Dangerous goods follow IMDG or IATA rules.

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.
30–42 daysOcean transit to Poti
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: Ministry of Environmental Protection and Agriculture (EU-aligned chemicals legislation).

Indicative total by sea: 37–59 days

By air: about 7–16 days in total.

Documents for Georgia

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Georgian-language labelling where required
Import permit for controlled precursors or narcotics where applicable
Transit declaration for onward cargo to neighbouring countries
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 Georgia

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

Full impurity reference standards range

3,5-Dihydroxybenzaldehyde

CAS: 26153-38-8
Formula: C₇H₆O₃
MW: 138.12 g/mol

ZX-036598

4-(N,N-Dimethylsulfamoyl)benzoic acid

CAS: 1206-37-7
Formula: C₉H₁₁NO₄S
MW: 229.26 g/mol

ZX-036599

2',3',5'-Tri-O-acetyl Guanosine

CAS: 6979-94-8
Formula: C₁₆H₁₉N₅O₈
MW: 409.35 g/mol

ZX-036600

Pirarubicin

CAS: 72496-41-4
Formula: C₃₂H₃₇NO₁₂
MW: 627.6 g/mol

ZX-036601

Vinflunine Ditartrate

CAS: 194468-36-5
Formula: C₅₃H₆₆F₂N₄O₂₀
MW: 1117.1 g/mol

ZX-036603

5-Acetoxy-3-chloro-2-pentanone

CAS: 13051-49-5
Formula: C₇H₁₁ClO₃
MW: 178.61 g/mol

ZX-036606

Chlorprothixene EP Impurity B

CAS: 2622-24-4
Formula: C₁₈H₁₉NS
MW: 281.4 g/mol

ZX-036607

2-Nitrophenyl Hydrazine

CAS: 3034-19-3
Formula: C₆H₇N₃O₂
MW: 153.14 g/mol

ZX-036608

Alpha-Yohimbine hydrochloride

CAS: 6211-32-1
Formula: C₂₁H₂₇ClN₂O₃
MW: 390.9 g/mol

ZX-036609

N-Boc-L-homophenylalanine

CAS: 100564-78-1
Formula: C₁₅H₂₁NO₄
MW: 279.33 g/mol

ZX-036610

Pyridoxal

CAS: 66-72-8
Formula: C₈H₉NO₃
MW: 167.16 g/mol

ZX-036611

3-Benzoyl-4-hydroxy-1-methyl-4-phenylpiperidine

CAS: 5409-66-5
Formula: C₁₉H₂₁NO₂
MW: 295.4 g/mol

ZX-036612

Questions

Impurity Reference Standards for Georgia

Can Zemixal deliver impurity reference standards to Georgia?

Yes. We ship by sea to Poti and Batumi, 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 Georgia?

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 Regulation Agency for Medical and Pharmaceutical Activities (Ministry of Health) is agreed with you at quote stage.

How long does delivery to Georgia take?

Allow 30–42 days for ocean transit or 3–6 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 Georgia

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

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