{"id":896,"date":"2026-03-30T19:41:20","date_gmt":"2026-03-30T19:41:20","guid":{"rendered":"https:\/\/zichorlifetech.com\/?page_id=896"},"modified":"2026-04-20T13:17:59","modified_gmt":"2026-04-20T13:17:59","slug":"company2","status":"publish","type":"page","link":"https:\/\/zichorlifetech.com\/es\/company2\/","title":{"rendered":"Company2"},"content":{"rendered":"
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about us <\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Zichor Life Tech Pvt. Ltd. was established in 2023 and became operational in August 2025. \nFounded by a team of three experienced doctors (Dr. Sathya, Dr. Chaitanya and Dr. Swetha). \nBuilt with a strong vision of saving lives through advanced medical solutions. \nSpecifically designed to support surgeons, incorporating their practical expertise and clinical insights. \nFocused on delivering high-quality, reliable, and effective surgical products.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Department Contacts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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MEET THE\nTEAM<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Dr. Chaithanya \n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Managing Director\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Dr. Sathyanarayana\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Director & CEO<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Dr. Swetha<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Director & CFO\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Rashmi Nair<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Chief International Business Officer<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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S M Narayan<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Head of HR <\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Jayanth Birari<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Head of Operation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Raghvendra<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Head of Quality<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Arun Kumar<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Head of Accounts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Rupesh Shimpi<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Graphic Designer<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Zichor Life Tech Pvt. Ltd. operates on a 3,50,000 sq. ft campus with a 25,000 sq. ft built-up area, featuring an 8,000 sq. ft Class 10,000 (ISO Class 7) clean room & Laminar air ow with Class 100 (ISO Class 5). This controlled environment maintains particle levels below 352,000 particles (\u22650.5 \u00b5m) per cubic meter, ensuring strict sterility and biocompatibility essential for medical device manufacturing. Our facility is equipped with advanced machinery, in-house laboratory and instrumentation setups, and dedicated R&D units. A team of highly skilled and competent professionals ensures precision, consistency, and uncompromised quality in every product we manufacture. <\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Our Foundation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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BUILT TO\nLAST<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Zichor Life Tech operates from a state-of-the-art biomedical research and manufacturing infrastructure designed to support development, validation, and commercialization of next-generation hemostatic solutions. Our facilities meet the highest international standards combining clean-room manufacturing, advanced analytical laboratories, and dedicated clinical simulation spaces under\none roof.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Core Capability\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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PRECISION\nAT SCALE<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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From raw material sourcing to finished product release, every step of our process is governed by a rigorous quality management system. Our infrastructure is built not just to produce but to ensure every unit that leaves our facility performs exactly as designed in the most critical moments a surgeon will face.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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01<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Clean-Room Manufacturing<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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ISO Class 7 and 5 certified clean-room\nenvironments for contamination controlled production of all hemostatic products and their components.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Analytical Laboratories<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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In-house testing for biocompatibility, sterility, shelf-life, and mechanical performance reducing time from bench to market without compromising rigor.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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03<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Cold Chain Logistics<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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End-to-end temperature-controlled distribution infrastructure ensuring product integrity from our facility to the operating room, every time.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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04<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Digital QMS Platform<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Fully digital quality management system covering document control, CAPA, deviation management, change control, and supplier qualification.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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13485 Compliant QMS<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Our quality management system is built to ISO 13485 the gold standard for medical device quality assurance globally.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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GMP<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Manufacturing Standard<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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All manufacturing processes adhere to Good Manufacturing Practice guidelines as defined by international regulatory authorities.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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24\/7<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Quality Monitoring<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Continuous environmental monitoring, automated batch record review, and real-time quality data dashboards always on.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Our R&D pipeline is grounded in a structured, phase-gated development process from in- vitro proof-of-concept through pre-clinical animal models to clinical validation in human surgical cases.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Research Foundation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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SCIENCE FIRST<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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No Zichor product reaches commercialization without rigorous, independent evidence of safety and efficacy. We collaborate with leading academic medical centers, hemostasis research laboratories, and clinical investigators across India and globally to ensure our science is both cutting-edge and clinically relevant. \nOur development process is physician-led at every stage from identifying unmet clinical need through designing study endpoints that reflect what actually matters to a surgeon at the table under pressure.<\/h2>\t\t\t\t<\/div>\n\t\t
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Coagulation-Independent Hemostasis<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Developing active hemostatic agents that achieve rapid clot formation independently of the patient's own coagulation cascade enabling effective bleeding\ncontrol in anticoagulated, thrombocytopenic, and coagulopathic patients.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Topical Bioadhesive Hemostats<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Engineering next-generation tissue-adhesive hemostatic dressings with superior wet-surface adhesion, biodegradability, and zero foreign-body reaction for\nboth open and laparoscopic applications.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Certification is not a checkbox it is the foundation of our promise to patients, clinicians, and healthcare systems. We pursue the most rigorous international regulatory standards as a reflection of our commitment to safety and quality.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Our Standards<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Our certifications span manufacturing quality, product performance, biocompatibility, and sterility covering every dimension of what it means to produce a safe, effective medical device that a surgeon can trust in the most critical moment of a patient's care.

\nCertification is ongoing, not static. We maintain an active post-market surveillance program and conduct regular internal and external audits to maintain compliance at all times.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Quality Management<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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ISO 13485:2016<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Medical devices quality management systems. Our QMS is\ndesigned, implemented, and maintained to meet the full\nrequirements of ISO 13485 \u2014 covering design controls,\nproduction, post-market surveillance, and customer\nfeedback.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Regulatory Compliance<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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CDSCO Registration<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Our products are developed and registered in compliance\nwith the Central Drugs Standard Control Organisation\nrequirements under the Medical Devices Rules, 2017 \u2014 India's\nprimary medical device regulatory framework.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Biocompatibility<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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ISO 10993 Series<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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All Zichor hemostatic products undergo comprehensive\nbiocompatibility evaluation per ISO 10993, including\ncytotoxicity, sensitization, irritation, and systemic toxicity\nassessments prior to any clinical use.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Sterility<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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ISO 11135 \/ 11137<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Sterilization validation performed per ISO standards for\nethylene oxide and radiation-based processes, ensuring\nevery product reaches the surgical field in a validated sterile\nstate without exception.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Manufacturing<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Schedule M GMP<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Our manufacturing facilities comply with the revised\nSchedule M Good Manufacturing Practice guidelines,\nensuring pharmaceutical-grade manufacturing rigor is\napplied to all hemostatic products we develop.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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International Markets<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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CE Mark In Progress<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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CE marking under EU MDR 2017\/745 is actively being\npursued for key products, enabling entry into European\nhealthcare markets and demonstrating alignment with the\nworld's most stringent device regulations.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Our goal is not just to achieve certification but to maintain it with integrity, year after\nyear. Every audit, every deviation, and every corrective action is an opportunity to make\nour quality system stronger and our products safer.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO+<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

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