“Saving lives through advanced and reliable medical solutions”
Founded by a team of experienced Doctors
Dr. Chaitanya, Dr. Swetha & Dr. Sathya the company is built on deep clinical expertise and a strong understanding of real-world surgical needs.
“Built for speed, compliance, and clinical impact, Zichor combines manufacturing excellence with surgeon-first innovation. Our mission is simple: deliver high-performance surgical products that compete globally—without compromise on quality, safety, or accessibility.”
Department Contacts
MEET THE TEAM
Dr. Chaithanya
Managing Director
Dr. Sathyanarayana
Director & CEO
Dr. Swetha
Director & CFO
Rashmi Nair
Chief International Business Officer
S M Narayan
Head of HR
Jayanth Birari
Head of Operation
Raghvendra
Head of Quality
Praveen B
Head of Supply Chain
Arun Kumar
Head of Accounts
Rupesh Shimpi
UI UX & Graphic Designer
INFRASTRUCTURE
Core Capability
PRECISION
AT SCALE
Total Campus
3,50,000 sq. ft
Built Up
25,000 sq. ft
Clean Room
8,000 sq. ft
Class 10,000 (ISO Class 7)
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.
01
100% Clean-Room Manufacturing
02
Analytical Laboratories
03
Inhouse R&D
04
Strong Regulatory Backing
ISO
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
Compliance
100% Regulatory Compliant
We ensure the facility is compliant with all the regulatory requirements to the highest standard
RESEARCH & DEVELOPMENT
Pipeline
structured phase-gated development
In- vitro proof-of-concept through pre-clinical animal models
Clinical validation in human surgical cases.
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.
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.
Research Foundation
SCIENCE FIRST
No Zichor product reaches commercialization without rigorous, independent evidence of safety and efficacy.
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.
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
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.