As a healthcare technology company, MEYRUSTM follows the classic methodology of product development. However, true to its business philosophy of Reaching MankindTM it optimizes the whole distribution network to help address the ‘last mile’ challenge in making affordable healthcare & healthy living a reality even in the remotest of the places.

Barring a few, most of our productions are outsourced to factories in South Korea, Malaysia, Thailand, India, Egypt & Turkey. However, we hold the intellectual property of technologies used to manufacture the products that we develop and some of those Intellectual Properties are now patent pending.

Production:

Key process:

XdureTM is a properietory formulation for latex compound that has an established track record of contributing to enhanced tensile strength and longer shelf-life. This formulation was initially developed and later fortified, to arrest attenuation factors to an extent, emerging from non-adherence to transport and storage conditions.

ProloTM  is a patent-pending process  & formulation re engineering to economize & enhance leaching efficiency by about 55%. This helps achieve great results without any significant rise in production cost.

R&D Life Cycle:

Consumers are at the center of all our research and development efforts. MEYRUSTM strives to innovate in science that will ultimately make a meaningful difference in people’s lives all over the world. Thanks to our market outreach, we have been receiving unprecedented amount of feedback from a variety of sources and are fast gaining experience in designing, formulating and developing novel array of products. Our R&D life cycles have shown remarkable success to develop/enhance products within the time frame.

Testing & pre-launching: Thanks to our strong institutional clients network, we have been able to greatly shorten the test phase before commercial launch of our products.

Post-launch surveillance: Our proactive market monitoring system collects structured feedback and analyze those with great accuracy to help determine the course or do a course correction if necessary. Product recall is, thus, always

Quality:

Our highest emphasis is always in providing zero-defect solution to our end-users. All Quality Control components are fine tuned to ensure that from the procurement of raw material to the delivery of the finished products, the issues of production wastage and supply of defective material are aptly addressed at every crucial stage.

For this, we only chose factories with state-of-the-art manufacturing facilities as our production partners. We also set and benchmark the important production parameters in cooperation with them to ensure optimal quality consistency.. batch after batch.

EN Conformity: CE

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Specifications: EN 455:2009 Part 1, 2, 3, 4

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Overview: MDR (EU) 2017/745)

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Specifications: US ASTM D3577

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Specifications: IN IS 13422

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Specifications: EN ISO 10282:2014

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Specifications: EN ISO 14644-1:1999

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Manufacturing: WHO-GMP

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KB5: Bioburden - High Pathogen Content & The Consequences

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Quality Management: ISO 13485:2016

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Quality Management: ISO 9001:2015

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KB9: Personal Protection: Latex Vs. Nitrile Vs. PolyIsoprene

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KB8: Importance Of Proper Disposal Of Used Gloves

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KB7: Importance Of Proper Gloves Packaging

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KB6: Sterilization - Ethylene Oxide Vs. Gamma Radiation

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KB4: Key Differences Between Long-Cuff Gyneocology & Long-Cuff Cleanroom Gloves

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Specifications: EN 374:2003, Part 1 & 2

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KB3: Key Differences Between Powdered And Powder-Free Gloves

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KB2: Why NeomexTM

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KB1: Why NeoglovTM

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Technical File: NEOMEXTM

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Technical File: NEOGLOVTM

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Specifications: EN 420:2003 + A1:2009

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