about us
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Department Contacts
MEET THE TEAM
Dr. Chaithanya N
Managing Director
Dr. Sathyanarayana R
Director & CEO
Dr. Swetha N
Director & CFO
Rashmi Nair
Chief International Business Officer
Raghvendra P.S.
Head of Quality
Jayanth Birari
Head of Operation
S M Narayan
Head of HR
Praveen B
Head of Supply Chain
Rupesh S
Graphic Designer
Arun Kumar S
Head of Accounts
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 (≥0.5 µm) 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.
Our Foundation
BUILT TO LAST
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 one roof.
Core Capability
PRECISION AT SCALE
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.
01
Clean-Room Manufacturing
ISO Class 7 and 5 certified clean-room environments for contamination controlled production of all hemostatic products and their components.
02
Analytical Laboratories
In-house testing for biocompatibility, sterility, shelf-life, and mechanical performance reducing time from bench to market without compromising rigor.
03
Cold Chain Logistics
End-to-end temperature-controlled distribution infrastructure ensuring product integrity from our facility to the operating room, every time.
04
Digital QMS Platform
Fully digital quality management system covering document control, CAPA, deviation management, change control, and supplier qualification.
ISO
13485 Compliant QMS
Our quality management system is built to ISO 13485 the gold standard for medical device quality assurance globally.
GMP
Manufacturing Standard
All manufacturing processes adhere to Good Manufacturing Practice guidelines as defined by international regulatory authorities.
24/7
Quality Monitoring
Continuous environmental monitoring, automated batch record review, and real-time quality data dashboards always on.
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.
Research Foundation
SCIENCE FIRST
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. Our 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.
Coagulation-Independent Hemostasis
Developing active hemostatic agents that achieve rapid clot formation independently of the patient's own coagulation cascade enabling effective bleeding control in anticoagulated, thrombocytopenic, and coagulopathic patients.
Topical Bioadhesive Hemostats
Engineering next-generation tissue-adhesive hemostatic dressings with superior wet-surface adhesion, biodegradability, and zero foreign-body reaction for both open and laparoscopic applications.
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.
Our Standards
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.
Certification 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.
Quality Management
ISO 13485:2016
Medical devices quality management systems. Our QMS is designed, implemented, and maintained to meet the full requirements of ISO 13485 — covering design controls, production, post-market surveillance, and customer feedback.
Regulatory Compliance
CDSCO Registration
Our products are developed and registered in compliance with the Central Drugs Standard Control Organisation requirements under the Medical Devices Rules, 2017 — India's primary medical device regulatory framework.
Biocompatibility
ISO 10993 Series
All Zichor hemostatic products undergo comprehensive biocompatibility evaluation per ISO 10993, including cytotoxicity, sensitization, irritation, and systemic toxicity assessments prior to any clinical use.
Sterility
ISO 11135 / 11137
Sterilization validation performed per ISO standards for ethylene oxide and radiation-based processes, ensuring every product reaches the surgical field in a validated sterile state without exception.
Manufacturing
Schedule M GMP
Our manufacturing facilities comply with the revised Schedule M Good Manufacturing Practice guidelines, ensuring pharmaceutical-grade manufacturing rigor is applied to all hemostatic products we develop.
International Markets
CE Mark — In Progress
CE marking under EU MDR 2017/745 is actively being pursued for key products, enabling entry into European healthcare markets and demonstrating alignment with the world's most stringent device regulations.
Our goal is not just to achieve certification but to maintain it with integrity, year after year. Every audit, every deviation, and every corrective action is an opportunity to make our quality system stronger and our products safer.
ISO+
We are committed to protecting the privacy and security of all personal data we collect and process. Full transparency on how we handle your information.
Privacy Policy
OVERVIEW
Zichor Life Tech ("we", "our", "the Company") is committed to protecting the privacy and security of all personal data we collect and process. This Privacy Policy explains how we collect, use, store, and protect your personal information when you interact with our website, products, or services.
This policy applies to all individuals whose data we process, including healthcare professionals, clinical partners, research collaborators, employees, and visitors to our digital platforms. We comply with applicable data protection laws, including the Digital Personal Data Protection Act, 2023 (India) and, where applicable, the GDPR (EU).
Last Updated: January 2025
DATA WE COLLECT
Identity & Contact Data
Name, title, professional registration number, email address, phone number, and institutional affiliation — collected when you register, contact us, or engage with our clinical programs.
Usage & Technical Data
IP address, browser type, device identifiers, pages visited, time on site, and referral source — collected automatically via cookies and analytics tools when you access our website.
Clinical & Research Data
De-identified or anonymized surgical outcome data, product feedback, and adverse event reports collected as part of our post-market surveillance obligations under applicable medical device regulations.
Communication Data
Records of correspondence, inquiries, and interactions with our medical affairs, sales, or support teams — retained for regulatory compliance and relationship management purposes.
HOW WE USE DATA
We process personal data only for legitimate, specified purposes and retain it only for as long as necessary. Our primary purposes include: fulfilling regulatory post-market surveillance requirements; communicating with healthcare professionals about our products; conducting clinical research and development activities; managing relationships with institutional and commercial partners; and improving our website and digital services.
We do not use personal data for unsolicited marketing without explicit consent, and we do not sell personal data to any third party under any circumstance.
DATA SHARING
Zichor Life Tech does not sell, rent, or trade personal data. We share data only where necessary to fulfill our obligations: with regulatory authorities (CDSCO, FDA, EMA) as required by medical device law; with contracted service providers operating under strict data processing agreements; academic and clinical research partners under formal data-sharing agreements; and where required by law or court order.
All third-party processors are contractually required to maintain data security standards equivalent to our own and to process data only for the specified purpose.
YOUR RIGHTS
You have the right to access personal data we hold about you; request correction of inaccurate data; request erasure where data is no longer necessary; object to or restrict certain processing activities; and lodge a complaint with the relevant data protection authority.
To exercise any of these rights, contact us at privacy@zichorlifetech.com. We will respond within 30 days of receipt of your request.
DATA SECURITY
We implement technical and organizational measures appropriate to the sensitivity of the data we process — including encryption at rest and in transit, role-based access controls, regular security audits, and mandatory data protection training for all staff.
In the event of a data breach that poses risk to individuals, we will notify affected parties and relevant authorities within the timeframes required by applicable law.
CONTACT US
For any privacy-related queries, data subject requests, or concerns about how we process your personal data, contact our Data Protection Officer:
Email: privacy@zichorlifetech.com Address: Zichor Life Tech Pvt. Ltd., bangalore karnataka
