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Philippines · Impurity Reference Standards

Impurity Standards supply to Philippines

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Philippines. Locally, the main users are in generic pharmaceuticals, electronics & semiconductor assembly and food & beverage. Regular consignments go to industrial centres such as Metro Manila, CALABARZON (Laguna, Cavite, Batangas) and Clark Freeport Zone. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

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

Supplying impurity reference standards to Philippines

By sea, containers and LCL lots take roughly 16–24 days to Manila (MICT) and Batangas. Air cargo to Manila Ninoy Aquino (MNL) takes 3–5 days, which suits small and urgent packs. The relevant authority is FDA Philippines. 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 Philippines

AuthorityFDA Philippines
SeaportsManila (MICT), Batangas, Cebu
AirportsManila Ninoy Aquino (MNL), Clark (CRK)
Dangerous goodsIMDG by sea, IATA DGR by air

Chemicals must appear on the Philippine Inventory of Chemicals and Chemical Substances (PICCS) or go through pre-manufacture notification with EMB-DENR. Substances on the Priority Chemical List, or covered by a Chemical Control Order, need registration and import clearance. APIs and drug products require FDA Philippines licensing of the importer, and dangerous drug precursors are licensed by PDEA. Dangerous goods follow IMDG or IATA rules, and AITIGA preference requires a certificate of origin.

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 Manila (MICT)

    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: EMB-DENR (PICCS, PCL / CCO).

Indicative total by sea: 23–41 days

By air: about 7–15 days in total.

Documents for Philippines

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • EMB-DENR PCL compliance certificate / CCO import clearance where applicable
  • FDA Philippines licence to operate / import authority for APIs where applicable
  • PDEA import permit for controlled precursors 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 Philippines

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 Philippines

Do you ship impurity standards to Philippines?
Yes. We ship by sea to Manila (MICT) and Batangas, 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 Philippines?
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 FDA Philippines is agreed with you at quote stage.
How long does delivery to Philippines 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.

Other divisions for Philippines

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

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