Manufacturing Manufacturing
Manufacturing
Our state-of-the-art oncology manufacturing facility is designed for precision, quality, and global compliance. We offer a full spectrum of services to support your business needs. Our advanced facilities and expert team ensure top-quality and efficient solutions tailored to your requirements.
Currently Installed Capacity Currently Installed Capacity
Currently Installed Capacity
- LAND AREA :- 24240 SQ FT METERS
- MANUFACTURING MORE THAN 400 FORMULATIONS & SKU’s
- CAPSULES :- 144 MILLION CAPSULES PER YEAR
- TABLETS :- 360 MILLION TABLETS PER YEAR
- LIQUID INJECTABLES :- 25 MILLION UNITS PER YEAR
- LYOPHILIZED INJECTABLES :- 5 MILLION UNITS PER YEAR
Quality Policy Quality Policy
Quality Policy
At Medion Biotech, quality is the cornerstone of everything we do. Our policy is built on a strong commitment to health, safety, environmental responsibility, and regulatory excellence.
- We integrate health, safety, and environmental protection into our overall quality strategy.
- We are committed to manufacturing and delivering high-quality oncology drugs that consistently meet the expectations of our valued clients and healthcare partners.
- We ensure strict adherence to cGMP and comply with all relevant national and international regulatory standards.
- We continually strive to enhance customer satisfaction through the ongoing improvement of our Quality Management System, aligned with ISO 9001:2015 standards.
Our goal is not just to meet expectations—but to exceed them, every step of the way.
Research & Development Research & Development
Research & Development
Medion Biotech's R&D infrastructure is built to support innovation, regulatory compliance, and product excellence. Our in-house chemical, instrumental, and microbiological laboratories are equipped with advanced technologies to ensure strict adherence to GLP standards.
We utilize cutting-edge instruments such as HPLC, FTIR, TOC Analyzer, UV Photometers, and various chromatographic techniques for accurate and reliable analysis.
Dedicated R&D and stability laboratories are in place, supported by real-time and accelerated stability chambers designed in compliance with ICH guidelines — enabling us to ensure product consistency, shelf-life, and regulatory readiness across global markets.
