Built for the precision, repeatability and documentation that pharma demands. SS316L, full GMP documentation, IQ/OQ support, validated CIP.
Pharmaceutical manufacturing runs on validation, repeatability and documentation. Every batch must match the last. Every cleaning cycle must be proven. Every material contact surface must be traceable.
Our RS series for pharma comes with full GMP documentation pack: material certificates (3.1), surface roughness reports, calibration certificates for instruments, factory acceptance test (FAT) videos, and IQ/OQ templates. We can also integrate validated CIP (clean-in-place) systems.
Steroid creams, antibiotic ointments, antifungal gels, pain relief creams.
Diclofenac gel, lidocaine gel, hormone gels, dermatological gels.
Oral suspensions, antibiotic syrups, antacid suspensions.
Glycerin bases, cocoa butter bases, PEG bases.
Antifungal creams, antiseptic creams, depilatory creams, sunscreen lotions.
Topical veterinary products, ear medications, wound sprays.
Contrast media prep, reagent suspensions.
Pre-formulation mixing, micronized suspensions, intermediate emulsions.
Every pharma machine ships with the documentation your QA team needs.
Send us your URS (User Requirement Specification) and we'll come back with a tailored spec, indicative price and full documentation plan.
Send Your URS →