- Assay / purity
- 99.0–101.0%
- MOQ
- 25 kg
- Lead time
- 7–15 days ex-stock
API · Intermediates · Veterinary · Packaging
Pharmaceutical raw materials, documented to the standard your QA team audits.
APIs, pharmaceutical intermediates, veterinary actives and primary packaging for generic manufacturers, CDMOs and qualified distributors. Every consignment ships with a CoA, an SDS and the regulatory file your market actually requires.
GMP manufacturing
DMF & CEP dossiers
Audit packs on request
67Products in the published library
42Countries supplied
17Years in pharma sourcing
6GMP sites audited
Materials · packaging · paperwork
The three things that actually cross the border
Before a consignment is released, your QA team reviews the material, the container it ships in and the batch documents that travel with it. These are the three layers, shown as illustrative photography of the material types we supply.
Four product lines
One supplier across the raw-material bill of your formulation
Buying an API, its intermediate and the vial it goes into from three different vendors triples your supplier qualification work. We keep the four lines under one documentation standard and one commercial contact.
20 products
Active Pharmaceutical Ingredients
Human-use actives with pharmacopoeial grades and per-batch CoA. DMF and CEP support for regulated markets.
Browse category
19 products
Pharmaceutical Intermediates
Building blocks and advanced intermediates for synthesis routes, supplied with GC/HPLC purity data and route notes.
Browse category
18 products
Veterinary APIs
Animal-health actives for antiparasitic, antibacterial and anticoccidial formulations, with MRL guidance.
Browse category10 products
Pharmaceutical Packaging
Primary packaging — glass, elastomer closures, blister film, foil and capsules — with extractables documentation.
Browse categorySelected products
Catalogue entries buyers ask for first
Each record lists the pharmacopoeial grade, the parameters we release against, the documentation pack and the minimum order. Specifications below are catalogue standards — your dossier specification always overrides them.
- Assay / purity
- 98.0–102.0%
- MOQ
- 5 kg
- Lead time
- 20–30 days
- Assay / purity
- ≥ 99.0%
- MOQ
- 1 000 kg
- Lead time
- 10–20 days
- Assay / purity
- 95.0–102.0%
- MOQ
- 1 kg
- Lead time
- 20–30 days
- Assay / purity
- 98.0–102.0%
- MOQ
- 25 kg
- Lead time
- 15–25 days
- Assay / purity
- Hydrolytic resistance HGA1
- MOQ
- 50 000 pcs
- Lead time
- 20–35 days
How buyers qualify us
Four questions decide whether a supplier gets a second order
Price wins the first purchase order. These four decide the next ten. We answer all of them before you ask.
- Is the documentation complete on arrival? A CoA that arrives two weeks after the drum stops your goods-inward release. Ours ships in the same carton, per batch, with method references.
- Does the next batch match the last one? Impurity profiles drift when a supplier switches route or site without telling you. We declare route and site changes before shipment, not after.
- Can your QA team audit the file you sent? DMF open part, CEP where one exists, nitrosamine risk assessment, TSE/BSE statement. If a document is missing, we say so rather than substituting a datasheet.
- Who answers when a batch is questioned? A named product manager with access to the batch record — not a shared inbox. OOS investigations get a technical response within one business day.
What ships with every consignment
- Certificate of AnalysisBatch-specific, tested against the agreed specification
- Safety Data SheetCurrent GHS revision, destination-language on request
- Regulatory statement packDMF / CEP reference, TSE/BSE, allergen and nitrosamine statements as applicable
- Packaging & transport recordNet weight, lot number, seal number, storage conditions
GMPISO 9001:2015ISO 14001DMF / CEP supportHalalKosher
How an order runs
From enquiry to commercial supply in four steps
No step is skipped for a new customer, and no step requires you to chase us for an update.
STEP 01
Enquiry & technical match
Send the CAS number, grade, target market and annual volume. We confirm the manufacturing site, the route and whether the grade you need is a catalogue item or a custom run.
STEP 02
Documentation review
Before any sample ships, you receive the open part of the DMF, a representative CoA and the regulatory statements for your destination market, so QA can qualify on paper first.
STEP 03
Sample & qualification
100 g to 1 kg samples for laboratory qualification, retained-lot reservation for the duration of your stability work, and a technical contact for method questions.
STEP 04
Commercial supply
Agreed release specification, packaging to your line requirement, shipping documents and a change-control notification before any process or site change.
Markets served
Documentation tuned to where the goods are released
The same molecule needs a different paper trail in Rotterdam than it does in Cairo. We prepare the file for the market of release, not for our own convenience.
- EuropeCEP & EU-GMP documentation, EDQM-aligned dossiers
- North AmericaUSDMF Type IV support, cGMP audit packs
- Latin AmericaANVISA / COFEPRIS registration assistance
- South & Southeast AsiaBulk supply with local release testing
- Middle East & AfricaTender-ready packs, Arabic labelling
Technical resources
Notes for the people who write the dossier
Short, practical briefings on supplier qualification and regulatory documentation — written for QA, regulatory affairs and procurement, not for search engines.
Supplier qualification
How to vet an API supplier before you place the first order
A practical sequence for qualifying a new API source when you have no audit history with them — what to request, in what order, and what each document actually proves.
Read note
Documentation
CoA vs SDS: what each document actually tells your QA team
These two documents arrive in the same envelope and get filed in the same folder. They answer completely different questions, and confusing them is a common source of audit findings.
Read note
Regulatory
CEP, USDMF or both? Matching the documentation pack to the destination market
The same API needs different paperwork in Europe, the United States and an emerging market. Here is how the three main routes differ, and where buyers over-specify.
Read noteNeed a specification, a sample or a price?
Send the CAS number, the grade your dossier requires and the annual volume. You will get a technical reply from the product desk — not a sales autoresponder.