From sterile production lines to analytical labs, Sri Anusham has supplied examination long cuff gloves to pharmaceutical and biotech companies for over 10 years. 100% made in India for reliable, uninterrupted supply.
Our state-of-the-art manufacturing facility, quality systems, and documentation processes are built for the stringent requirements of pharmaceutical and biotech companies.
Two core materials. Multiple sterility and packaging configurations. Every variant engineered for the controlled environments of pharma and biotech manufacturing.
EN 374 Type B chemical resistance — certified barrier against industrial chemicals and solvents
100% latex-free and protein-free — eliminates Type-I allergy risk and contamination risk
Advanced double-chlorination — smooth donning, efficient double-donning for high-risk protocols
Superior puncture resistance compared to natural rubber latex
FDA 21 CFR 177.2600 compliant — dual-use for food-contact and pharma applications
Nitrosamine-free & anti-static variants available on request
Superior elasticity and tactile sensitivity — preferred for precision handling of tablets, capsules, and delicate formulations
Advanced double-chlorination — effortless donning and efficient double-gloving protocols
EN 374 Type B chemical resistance certified
FDA 21 CFR 177.2600 compliant for food contact applications
AQL 0.65 — 100% individual quality inspection before packaging
We know that in pharma procurement, trust is built on documentation. Here is the compliance infrastructure behind every glove we ship.
Common questions from quality managers and procurement teams in pharma and biotech.
Every shipment comes with a Certificate of Analysis (CoA) and Certificate of Conformance (CoC) per batch. Additional documentation available includes an MSDS, TDS, equipment calibration records, and a Master List of SOPs. Our centralised QA documentation system ensures fast access to compliance records for any customer query or audit.
Our PharmShield examination gloves comply with ISO 13485:2016, ISO 9001:2015, CE PPE 2016/425 Type B compliance, EN 455 Parts 1–4, EN 374 (chemical resistance), ISO 10993 (biocompatibility), ISO 11193, and ASTM D3578 (Latex) / ASTM D6319 (Nitrile). The facility is CDSCO-certified and compliant with BIS (IS 13422) and FDA requirements. Sterile variants are validated to ISO 11737-1 & 2 with a 10⁻⁶ SAL.
Yes. PharmShield Nitrile and Latex Gloves are EN 374 Type B certified, providing a verified barrier against a wide range of industrial chemicals and solvents. Detailed permeation data per EN ISO 16523-1 is available to support your process risk assessment.
Both our nitrile and latex PharmShield examination gloves are available in Non-Sterile, ETO (Ethylene Oxide), and Gamma Irradiation Sterile variants. Sterile gloves achieve a Sterility Assurance Level (SAL) of 10⁻⁶ and are validated per ISO 11737-1 & 2. Packaging options include dispenser box, individual pack, vacuum pack, and triple vacuum pack.
Yes. We provide complete registration packs and documentation to streamline your vendor approval process. Our centralised QA documentation system ensures fast access to compliance records for customer queries. As a 100% in-house manufacturer operating for over 35 years, we offer the supply reliability and documentation depth that pharma procurement teams require. We are also ready to facilitate customer audits.
Contact us to request samples or get expert recommendations for your specific pharmaceutical and biotech needs.
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