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Taiwan · Impurity Reference Standards

Impurity Reference Standards for Taiwan

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Taiwan. In Taiwan the strongest demand is from semiconductors & electronics, petrochemicals and pharmaceuticals. Typical delivery points include Hsinchu Science Park, Kaohsiung (Linyuan, Renwu) and Taichung / Central Taiwan Science Park. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

20,060products in this division
16–24 dsea transit from India
3–5 dair freight
6categories

Supplying impurity reference standards to Taiwan

Sea freight reaches Kaohsiung and Keelung in about 16–24 days port to port. Urgent or small lots fly to Taipei Taoyuan (TPE) in 3–5 days. Import compliance for this category sits with TFDA, 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 Taiwan

AuthorityTFDA
SeaportsKaohsiung, Keelung, Taichung
AirportsTaipei Taoyuan (TPE), Kaohsiung (KHH)
Dangerous goodsIMDG by sea, IATA DGR by air

Under the Toxic and Concerned Chemical Substances Control Act (TCSCA), administered by the Ministry of Environment, new and certain existing chemical substances must be registered, and listed toxic or concerned substances need permits or approvals before import. The Ministry of Labor runs a parallel registration scheme under the Occupational Safety and Health Act. Traditional Chinese SDS and labels are expected and are usually prepared by the importer. APIs need TFDA registration and DMF review. Dangerous goods follow IMDG or IATA rules.

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. 16–24 daysOcean transit to Kaohsiung

    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: MOENV (TCSCA) / MOL (OSHA chemical registration).

Indicative total by sea: 23–41 days

By air: about 7–15 days in total.

Documents for Taiwan

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • TCSCA registration / toxic or concerned chemical permit where applicable
  • Traditional Chinese SDS / label (prepared by importer)
  • TFDA API registration / DMF documents where applicable
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

A selection we ship to Taiwan

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 Taiwan

Can Zemixal deliver impurity reference standards to Taiwan?
Yes. We ship by sea to Kaohsiung and Keelung, 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 Taiwan?
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 TFDA is agreed with you at quote stage.
How long does delivery to Taiwan take?
Allow 16–24 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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