Pharmaceutical glass — regulatory precision, particle inspection, full traceability.
USP Type I/II/III, EP standards, vial and ampoule precision, regulatory traceability.
The shape of this industry's hot end.
Borosilicate (Type I) for parenterals · soda-lime (Type II/III) for orals · particle/visual inspection at full lot · regulatory audit-ready.
What we see most often in pharma.
Specifications that drive the floor.
USP <660>, <1660>, <87>, <88>, <381> · EP 3.2.1 · ISO 4802 · 21 CFR Part 11 traceability · cGMP compliance.
Who the segment serves.
Schott, Gerresheimer, SGD Pharma, Stevanato Group, Nipro, plus pharma OEMs (J&J, Pfizer, Roche, GSK, Novartis, AstraZeneca).
Lean Glass services for pharma plants.
Hot End Audit
Independent audit of IS machines, forehearth, hot-end coating, ware handling and pack-to-melt KPIs.
Forming Audit
Section timing, mould equipment, NNPB/BB/PB process control and defect taxonomy linked to root cause.
Job Change Tool
The world's first systemised Job Change Tool — SKU Library · Live Execution · KPI Tracking.
Digitalisation & Reporting
Live KPI dashboards, hot-end/cold-end data integration, digital audits, real-time defect tracking.
Questions, answered.
Yes. Engagements run with full traceability and align to your QMS.
30-minute call with a senior practitioner.
Bring a problem — leave with a direction.