Gennex Laboratories
Our cutting-edge facility is centrally situated in Hyderabad and boasts a comprehensive manufacturing setup. Featuring a state-of-the-art Quality Control Lab and Industry Leading Quality Assurance protocols, our facility has a capacity exceeding 85KL.
We routinely undergo and successfully pass audits conducted by customers and various Ministries of Health (MOH).
We hold numerous certifications, both domestically and from various international markets, including, but not limited to, Indian GMP, WHO GMP and COFEPRIS. Furthermore, we continuously upgrade and update our Facility and Processes to meet the standards required for any of our clients globally.
Our Quality Policy
- State of Art Quality Control Laboratory is provided with in industry practice with relevant experience.
- Well equipped State of the Art Analytical Instruments.
Quality Systems
Quality
Ensuring the highest standards of quality in every aspect of manufacturing, from raw materials to finished products, to deliver safe and effective medications to patients.
Integrity
Conducting business with honesty, transparency, and ethical practices, adhering to regulatory guidelines and maintaining the trust of customers, healthcare professionals, and stakeholders.
Customer Focus
Placing customers at the center of operations, understanding their needs, and providing exceptional products and services that meet their expectations and improve their healthcare outcomes.
Innovation
Embracing research and development, investing in new technologies, and continuously seeking improvements in manufacturing processes to bring innovative and effective medications to the market.
Compliance
Adhering to strict regulatory requirements, staying up-to-date with industry standards, and maintaining a robust compliance program to ensure the safety, efficacy, and legality of all products.
Collaboration
Fostering partnerships and collaborations with healthcare professionals, suppliers, and stakeholders to drive mutual success, share knowledge, and collectively contribute to the advancement of healthcare.
Sustainability
Operating in an environmentally responsible manner, promoting sustainable practices, minimizing waste, and striving to reduce the environmental impact of manufacturing operations. We are a zero waste facility with facility output in compliance as per Central Effluent Manufacturing system.
Quality Assurance
Our Quality Team is fully independent of manufacturing and adopting advanced standards of techniques acceptable globally.
Quality Assurance is responsible for the implementation of integrated Quality Systems. It harmonizes global quality and regulatory standards across the functions with a collective collaboration.Our CERTIFICATIONS
Our facilities is WHO-GMP certified by the CDSCO / State Drug Control Authority and the manufacturing facilities are certified by TUV NORD for ISO 9001:2015, ISO 14001:2015 and ISO 45001:2008.
