Nuclear medicine departments
Cold kits, labelling precursors and generator supply, scheduled around your licence and delivery windows.
APIChemX is a supply chain intelligence and supply chain partner for active pharmaceutical ingredients, specialty chemicals and the inputs behind nuclear medicine. Search products, share your requirements and coordinate quotations, documents and delivery through APIChemX.
Every enquiry gets the same treatment: a screened request, a verified manufacturer and a document pack you can file.
Labelling precursors such as PSMA-617 and DOTATATE, chelators, cold kits and generator supply, coordinated with your licence and delivery window.
Explore APIs and build a quotation request with the grade, quantity, documents and destination you need.
Directory listings are self-reported. A GMP claim, a DMF number or a site address can be years out of date.
CoAs, DMF letters of access and TSE/BSE statements often arrive after payment, when it is too late to walk away.
A gallium-68 generator or a lutetium-177 shipment loses activity every hour a customs file sits incomplete.
Quotes arrive without grade, Incoterm or lead time, so two prices for the same molecule rarely mean the same thing.
Clinical and pilot batches need grams to a few kilograms. Many producers only quote by the drum.
Scarce molecules often have one active manufacturer. One audit finding can stop supply for months.
| What matters | Typical open directory | APIChemX |
|---|---|---|
| Supplier identity and GMP status | Self-reported by the listing | Checked against public registers before every quote |
| Document pack | Usually requested after the order | CoA, SDS, filings and GMP certificate reviewed first |
| Molecules nobody lists | Only what a seller has posted | Searched at the manufacturer, listed or not |
| Radioactive material | Not treated differently | Licensed producer to licensed receiver only |
| Point of contact | One conversation per supplier | One thread from enquiry to delivery |
You send the molecule, grade, quantity, documents and destination, on WhatsApp or through the enquiry form.
We confirm the specification, the regulatory requirements of your market and your licence where one is needed.
We shortlist manufacturers and check GMP status, regulatory filings and recent CoAs against public registers.
You receive comparable offers with lead time, Incoterm and the document pack already reviewed.
We coordinate samples, contracts, shipping and customs paperwork, and stay on the thread until the goods are released.
Cold kits, labelling precursors and generator supply, scheduled around your licence and delivery windows.
GMP peptide precursors, chelators such as DOTA and NOTA derivatives, and reference standards for method validation.
Second sources for APIs with thin supply, with DMF or CEP access and pharmacopoeial grades.
Gram-scale quantities of recent kinase inhibitors and cytotoxics, with CoA and HPLC data.
Catalysts, reagents, high-purity solvents and chiral building blocks matched to your specification.
Back-to-back sourcing with export documents, agreed Incoterms and consolidated shipments.
Sourced in 69 countries.
Moved by air.sea.road.
UN class 7 for radioactive consignments through carriers that accept them. Class 6.1, 8 and others for hazardous chemicals, with the SDS on file.
2–8 °C and frozen shipments for peptides, kits and biologic precursors, with data loggers where the receiver needs them.
Commercial invoice, packing list, certificate of origin and import permits agreed before dispatch, not after arrival.
Send the molecule and the quantity. We reply with what we can confirm, what we still need from you, and a realistic lead time.