The pharmaceutical and cosmetics industries require conveyors that operate in validated, controlled environments where contamination control, traceability, and regulatory compliance are non-negotiable. Equipment must integrate with cleanrooms and undergo rigorous IQ/OQ qualification.
Jumak designs GMP-compliant conveyor systems with FDA 21 CFR-grade materials, electropolished stainless steel (Ra ≤ 0.8 μm), and sealed, low-particulate drives. Systems come with full validation documentation supporting ANVISA and FDA audits.
Full compliance with cGMP, FDA 21 CFR, and ANVISA requirements with validated documentation.
Designed for ISO Class 7/8 cleanrooms with sealed drives, smooth surfaces, and low-particulate belts.
Complete Installation and Operational Qualification packages with material certificates and weld reports.
Electropolished stainless steel with Ra ≤ 0.8 μm for pharmaceutical-grade smoothness and cleanability.
Integration with vision systems, barcode readers, and serialization systems for track-and-trace compliance.
Precision speed control and cushioned transfers for fragile vials, ampoules, and cosmetic containers.
Yes. Designed for ISO Class 7 and 8 cleanrooms with smooth, particle-free surfaces, sealed drives, and low-particulate belt materials.
IQ/OQ packages, FDA 21 CFR material certificates, surface finish reports (Ra ≤ 0.8 μm), and weld inspection records supporting ANVISA and FDA audits.
Request a no-obligation quote and receive a customized proposal for your operation.