Premium cleanroom gloves engineered for pharmaceutical manufacturing, sterile compounding, and isolator systems. ISO 14644-1 compliant, EU GMP certified, FDA approved.
Request QuotePharmaceutical manufacturing demands the highest standards of contamination control, sterility, and regulatory compliance. Sterimed gloves are specifically designed to meet these rigorous requirements.
Every glove undergoes thorough quality inspection to ensure AQL 1.5 standards, providing the reliability pharmaceutical manufacturers require.
Full compliance with EU Good Manufacturing Practice regulations, ensuring your products meet European market requirements.
Gloves suitable for Class 10, 100, 1,000, and 10,000 cleanroom environments, meeting ISO 14644-1 particle count standards.
Gamma and ETO sterilization available, with validated processes ensuring sterility assurance levels (SAL) of 10^-6.
US FDA approved for use in pharmaceutical manufacturing, meeting 21 CFR Part 820 quality system regulations.
Medical Device Regulation (MDR) 2017/745 compliant, with CE marking for European market access.
Class 10-10K • AQL 1.5 • Powder Free
Class 10-10K • AQL 1.5 • Powder Free
400mm/480mm • ETO Sterilized • Isolator Systems
400mm/480mm • Chemical Resistant • Isolator Systems
400mm/480mm • Superior Sensitivity • Isolator Systems
Sterile Latex • Powder Free Polymer Coated • Surgical Grade
Sterimed maintains comprehensive certifications required for pharmaceutical manufacturing:





Contact Sterimed to discuss your pharmaceutical glove requirements. Our team can help you select the right products for your specific application and ensure compliance with all regulatory requirements.