Stainless steel fabrication for the pharmaceutical industry
ADI fabricates stainless steel parts, components and equipment for pharmaceutical environments where compliance, traceability and surface finishes are critical. CWB and ISO 9001 certified.
Fabrication challenges for pharmaceuticals
Strict GMP standards
Manufacturing aligned with industry standards for sanitary equipment. Every part is produced using controlled, documented processes.
Specific surface finishes
Polishing and brushing adapted to prevent contamination. Our finishes meet the requirements of pharmaceutical environments and cleanrooms.
Material traceability
Rigorous tracking of steel origin and components used. Recorded inspection before each shipment to support immediate recall if non-conformance is found.
Complete documentation
Quality reports, material certificates and CWB and ISO 9001 certifications provided with every delivery.
Our services for the pharmaceutical industry
Questions about pharmaceutical fabrication
Do you comply with GMP standards?
Our processes are certified CWB Division 2 and ISO 9001. Every order includes documented inspection and full material traceability. Surface finishes are adapted to the sanitary requirements of the pharmaceutical sector.
What surface finishes do you offer for pharma?
Pharmaceutical- and medical-grade polishing and brushing. Our teams have developed specific expertise in anti-contamination finishes on piping, transitions and process equipment.
Do you provide traceability documentation?
Yes. Inspection reports, material certifications, and CWB and ISO 9001 compliance. Parts are identified and recorded before delivery.