Precision Engineered, cGMP Compliant
At RARA Pharmatech & Surgicals, quality is a non-negotiable metric. Our engineering processes are built on strict guidelines that guarantee durability, hygiene, and full compliance with ISO 9001:2015 and cGMP standards.
Since controlled cleanrooms and sterile environments cannot tolerate surface contamination, weld porosity, or chemical degradation, we run exhaustive checks at every single phase of our production workflow.
Our Quality Protocol
Material Verification
We source stainless steel sheets (SS304, SS316, SS316L) exclusively from certified mills. Every batch is accompanied by Mill Test Certificates (MTC) and undergoes chemical testing to confirm exact alloy percentages.
Welding Integrity Checks
Our TIG welds are verified to ensure complete penetration and a smooth profile. We inspect for weld porosity, cracking, and undercut. All joins are ground smooth to create crevice-free surfaces that prevent germ accumulation.
Surface Finish Profiling
Using portable surface roughness testers (profilometers), we verify the Ra values of electropolished or satin surfaces to ensure they meet the specific pharmaceutical cleanliness specifications (typically Ra < 0.8 μm).
Performance Testing
Active systems, like Laminar Air Flow hoods and Pass Boxes, are subjected to strict velocity mapping, HEPA filter integrity checks (PAO test), and particle count validation in accordance with ISO 14644-1 guidelines.
