zichorlifetech

About Us — Zichor Life Tech
Company Information

ABOUT
US

Everything you need to know about Zichor Life Tech — our infrastructure, research, certifications, privacy practices, and terms of service. One page. Full transparency.

2023
Physician-Founded
Mumbai, India
Infrastructure Research Certification Privacy Terms of Service Haemostatic Innovation Infrastructure Research Certification Privacy Terms of Service Haemostatic Innovation
Section 01
INFRASTRUCTURE

Our manufacturing backbone, quality systems, and operational infrastructure — built to meet the highest global standards for medical device development and production.

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 8 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.
Section 02
RESEARCH

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.

SCIENCE
"Every Zichor product begins with a clinical question and ends with a peer-reviewed answer. We build only what the evidence supports."
— Zichor Life Tech Research Philosophy
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.

01
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.
Active Research
02
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.
Pre-Clinical
03
Trauma Packing Solutions
Field-deployable hemostatic packing agents optimized for high-flow arterial and venous bleeding in military, mass casualty, and pre-hospital emergency settings.
Development
04
Biomarker-Guided Hemostasis
Exploratory research into intraoperative biomarker diagnostics to enable real-time, personalized hemostatic management during complex surgical procedures — the future of precision surgery.
Discovery
Section 03
CERTIFICATION

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

CERTIFIED
TO THE
HIGHEST
STANDARD

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+
Section 04
PRIVACY

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.

Contents
Overview
Data We Collect
How We Use Data
Data Sharing
Your Rights
Data Security
Contact
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
01
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.
02
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.
03
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.
04
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; with 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., Mumbai, Maharashtra, India

Section 05
TERMS OF
SERVICE

Our terms govern all use of the Zichor Life Tech website and digital platforms. By accessing our website, you agree to be bound by these terms.

Sections
1. Agreement to Terms
2. Use of Website
3. Intellectual Property
4. Medical Disclaimer
5. Limitation of Liability
6. Product Information
7. Governing Law
8. Contact
Section 01
AGREEMENT TO TERMS

By accessing and using the Zichor Life Tech website (zichorlifetech.com) or any of our digital platforms, you agree to be bound by these Terms of Service. If you do not agree to these Terms, please discontinue use of our website immediately.

These Terms constitute a legally binding agreement between you and Zichor Life Tech Private Limited, a company incorporated under the laws of India. We reserve the right to modify these Terms at any time. Continued use of the website following any modification constitutes acceptance of the revised Terms.

Section 02
USE OF WEBSITE

You may access and use this website for lawful purposes only. You agree not to use this website in any manner that could damage, disable, overburden, or impair its operation; transmit any harmful, offensive, or unlawful material; attempt unauthorized access to any part of our systems or data; or misrepresent your identity or professional credentials.

We reserve the right to terminate or restrict access to this website at our sole discretion, without notice, for any conduct we determine to be in violation of these Terms or harmful to other users, our business, or third parties.

Section 03
INTELLECTUAL PROPERTY

All content on this website — including but not limited to text, graphics, logos, product images, clinical data, and software — is the proprietary intellectual property of Zichor Life Tech or its licensors and is protected under applicable copyright, trademark, and patent laws.

No content may be reproduced, distributed, modified, publicly displayed, or used in any derivative work without the prior written consent of Zichor Life Tech. Limited personal, non-commercial use is permitted provided that all copyright and proprietary notices are retained intact.

Section 04
MEDICAL DISCLAIMER

The information provided on this website is intended for healthcare professionals and is for general informational purposes only. It does not constitute medical advice, diagnosis, or treatment recommendations, and should not be used as a substitute for professional medical judgment.

Product information, clinical data, and regulatory status described on this website may vary by country or region. Always refer to the approved labeling and Instructions for Use specific to your jurisdiction. Zichor Life Tech products must only be used by qualified healthcare professionals in accordance with their approved indications.

Section 05
LIMITATION OF LIABILITY

To the fullest extent permitted by applicable law, Zichor Life Tech shall not be liable for any indirect, incidental, consequential, special, or punitive damages arising from your use of this website or reliance on any information contained herein — including, without limitation, damages for lost profits, data loss, or business interruption.

Our total liability for any claim arising from your use of this website shall not exceed INR 10,000 or the amount paid by you (if any) for access to any specific service or content.

Section 06
PRODUCT INFORMATION

Product descriptions, clinical claims, and technical specifications on this website represent current information as of the date of last update. Zichor Life Tech makes no warranty regarding the completeness, accuracy, or timeliness of this information.

Regulatory approval status and product availability vary by market. Products described as "in development" or "pending regulatory approval" are not commercially available and should not be represented as cleared or approved for clinical use until official regulatory authorization has been obtained and communicated.

Section 07
GOVERNING LAW

These Terms shall be governed by and construed in accordance with the laws of the Republic of India, without regard to its conflict of law provisions. Any dispute arising under these Terms shall be subject to the exclusive jurisdiction of the courts of Mumbai, Maharashtra, India.

If any provision of these Terms is found to be unlawful, void, or unenforceable, that provision shall be deemed severable and shall not affect the validity and enforceability of the remaining provisions.

Section 08
CONTACT

For any questions regarding these Terms of Service, please contact:

Zichor Life Tech Private Limited
Legal Affairs | Mumbai, Maharashtra, India
Email: legal@zichorlifetech.com
Website: www.zichorlifetech.com

CONNECT
WITH US
Zichor Life Tech — Mumbai, India
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