We are not your supplier on this work. That is exactly why you can trust what we tell you about them.
You can find a supplier in an afternoon. What you cannot do from another country, in another language, is establish whether that supplier is what it claims to be, whether the certificate they sent you is real, and whether the documentation will survive contact with your regulator.
That is the gap this service exists to close. Send us the supplier, the order or the documents. We check the factory, we check the goods, and we read the paperwork properly. Then we tell you what is real, what is missing, and what will not satisfy your market.
We do not certify. NJMC is not a certification body and not a notified body. We provide independent verification and due diligence reports based on documentary review, factory checks and technical assessment. The conclusion is ours, the decision remains yours.
A supplier verifying their own goods is marking their own homework. A general inspection agency can count cartons and photograph pallets, but cannot read an impurity profile, cannot tell you whether a polymorphic form will survive your process, and cannot judge whether a dossier supports your filing route.
The work is done by a working biomedical scientist with two doctorates, based in Nanjing, operating in English, Arabic and Chinese. That combination is the reason this service exists at all.
Our fee is payable whether the answer is yes or no. It is never conditional on you buying anything afterwards, from us or from anyone else. If it were, the report would be worth nothing.
Whether the counterparty manufactures or trades. Whether the business registration is real. Whether the site named on the GMP or ISO certificate is the site that would actually produce your order, which is the single most common gap we find.
Certificate of analysis read against your specification rather than glanced at. GMP certificate checked for site, scope and expiry. Drug Master File and letter of access. CEP verified against the EDQM register. FDA listings checked against the public database. Stability data, which is the item most often missing from a package that otherwise looks complete.
Before shipment, confirming that what is loading matches the documentation you approved. Being physically in China is what makes this possible, and it is the check buyers most often skip because everything looked correct at quotation.
| Service | What you get | Introductory |
|---|---|---|
| Supplier Verification Report | Manufacturer or trader, registration and certificate checks, site identity, red flags, and a clear go, caution or no-go. | USD 150 |
| Pre-shipment Verification | Physical check in China before goods leave, matched against the approved documentation. | USD 250 |
| Dossier and Document Review | Full technical review of the COA, specification and regulatory package, with a gap list of what to demand before you commit. | USD 350 |
Introductory rates apply to the first ten engagements. Standard rates are USD 300, 500 and 750. Retainers are available where verification is needed regularly.
We source APIs, excipients, consumables, devices and equipment, and we have done so for many customers. Verification is a separate service for buyers who already have a supplier and want an independent opinion before they commit. You can use one, the other, or both. If you engage us to verify a supplier you found yourself, we have no stake in the outcome, and that is the point.
Send the product or molecule, the grade, the quantity and the destination market. You will get a considered answer about what can be sourced and what documentation comes with it.