What Gets Checked

Beyond whether the company legally exists.

Company verification (CIN, GST, registered address) confirms a business is real. It says nothing about whether that business can manufacture your product, at your volume, repeatably. That's a separate, technical question.

01

Manufacturer or Trader

Where the reactor is, who controls the formulation, and whether "we manufacture" means producing the chemistry or standardising a bought-in intermediate.

02

Plant & Process Capability

Equipment on the floor, batch size range, and whether the process that made the sample is the same one that would run commercial volume.

03

Laboratory & QC Capability

What the lab can actually measure on-site versus what it sends out, and whether QC data on a spec sheet reflects real instrumentation.

04

Documentation Quality

Whether batch records, COAs, and SDS revisions are maintained as a real practice or produced on request.

05

Repeatability

Evidence — where it exists — that this manufacturer's output is consistent lot to lot, not just that one sample was good.

06

Export Readiness

Packaging, labelling, and documentation practice matched against what your shipment and destination actually require.

Where This Sits

After the specification exists, before the order is placed.

Supplier Qualification assumes a target specification — from Technical Development or your own — and verifies the manufacturer against it. Once a supplier is qualified and in commercial production, BatchGate is what keeps every subsequent batch accountable to what was approved.

Scope, Stated Plainly

A point-in-time technical opinion, not a certification.

Supplier Qualification is Nython's documentary and/or on-site review of what a candidate manufacturer can demonstrate at the time of assessment. It isn't an audit against a named standard unless the engagement specifies one, and it isn't a guarantee of future performance.

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