- Pharma Furniture
GMP-compliant SS furniture with specified grades, Ra finishes, and crevice-free welds.
- Service Overview
Pharmaceutical manufacturing environments impose three specific requirements on furniture that most suppliers fail to satisfy simultaneously: material grade selected by CIP chemistry and GMP classification (not cost), surface finish specified by Ra value (not appearance), and weld joints that are genuinely crevice-free. Kurveline is an experienced pharma furniture manufacturer — having supplied to Pfizer, Dr. Reddy’s Laboratories, and Laurus Labs.
GMP SS workbenches, pharma lab furniture, storage cabinets, material trolleys, SS wash stations, pass boxes, QC lab benches, garment storage, and instrument storage for pharmaceutical manufacturing and quality environments.
- SS 316 for CIP and product-contact areas — SS 304 for dry cleanroom non-contact zones
- Surface finish to Ra ≤ 0.8 μm on product-contact surfaces — verifiable and documented
- Crevice-free weld finish on all GMP contact joints — probe-inspected, not just visually assessed
- Dimensions fabricated to your cleanroom layout — not catalogue standard sizes
- GMP documentation package available for QA approval
Capabilities
| Parameter | Specification |
|---|---|
| Materials | SS 316 for CIP and product-contact surfaces; SS 304 for dry cleanroom storage and non-contact areas |
| Surface Finish | Ra ≤ 0.8 μm product-contact surfaces; Ra ≤ 1.6 μm non-contact SS surfaces |
| Weld Finish | Crevice-free, ground and polished on all GMP contact joints |
| Pharma Lab Furniture | QC lab benches, instrument storage, reagent racking, analytical area workstations |
| Standards Awareness | Schedule M (India), WHO GMP, ISO 14644 cleanroom classification |
| Documentation | Material certificates (heat traceability), dimensional records, Ra verification |
Applications
Pharmaceutical Manufacturing
Primary and secondary manufacturing areas under Schedule M and WHO GMP
Pharma Lab
QC and R&D laboratory environments requiring GMP-compliant pharma lab furniture
Sterile Manufacturing
Fill-finish, lyophilisation, and aseptic areas requiring highest GMP surface standards
API Processing
Active pharmaceutical ingredient processing areas requiring SS 316 chemical resistance
Customization
Material grade (SS 304 or SS 316 by CIP chemistry and area classification), surface finish Ra value, crevice-free weld specification, dimensions from facility layout drawings, shelf configuration, door type, locking, quantity, and GMP documentation requirement can all be specified.
Our Process
Facility Drawing / GMP Spec
Facility drawings, dimensions, and GMP requirements received from the client.
Material & Grade Confirmation
SS 316 or SS 304 selected by area, with material certificates confirmed.
Fabrication
Lab furniture cut, formed, and welded to the facility drawings.
Surface Finishing
Surfaces ground and polished, with GMP contact joints made crevice-free.
Weld & Ra QC
Welds, dimensions, and Ra values checked against the specification.
Documentation & Delivery
Material certificates and inspection records supplied with the delivered units.
Quality & Engineering
Pharma furniture inspection covers: dimensional accuracy, Ra surface finish (verification available on request), crevice-free weld quality on all contact joints, hardware fitment, and material grade certificate. GMP documentation package for QA approval process available. Clients: Pfizer, Dr. Reddy’s Laboratories, Laurus Labs.