Pharmaceutical & Biotech

Audit-ready glass for GMP environments

USP <31> compliant volumetric ware with individual certificates your QA team can verify online during an audit — no email chains, no scanned PDFs from three years ago. Amber lines for photosensitive APIs, Type I glass documentation for stability studies.

What this programme includes

  • 01USP <31>/<660> documentation on file
  • 02Serialised instruments, online-verifiable
  • 03Amber volumetric range for photosensitive work
  • 04Change-control notification on process changes

Proof, not promises

A top-5 Indian formulations exporter standardised 14 QC labs on our serialised Class A line after a single MHRA audit closed with zero glassware observations.
Discuss your requirement

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