True to our commitment to improve patients’ lives and solve some of medicine’s most difficult challenges, Glenmark’s dedicated employees and state-of-the-art manufacturing centres help make our vision a reality. We have the scale and diversity to invest wisely in infrastructure and technology in order to ensure the uncompromised quality of and accessibility to medicines while controlling production costs.
In a highly regulated environment, where quality and precision are critical, our manufacturing processes are as rigorous as our scientific research. Our state-of-the-art global facilities include all the processes needed to manufacture safe products for our consumers.
All of our products are manufactured in accordance with the relevant regulatory agency’s regulations on good manufacturing practices.
Globally, Glenmark has
facilities in the
US, Europe and Asia
Quality and Compliance
At Glenmark, we operate an efficient and agile integrated organization that is committed to reinvesting for growth. Operating in high-quality–conscious regulated markets, we apply internationally recognised Good Manufacturing Practices (GMP) to ensure quality and safety. This covers all aspects of manufacturing, including standard operating procedures, personnel management and training, equipment maintenance and handling of materials.
Every person who participates in manufacturing activities for, or on behalf of, Glenmark is required to receive appropriate training; adhere to all applicable laws, regulations, policies and procedures; exert due diligence in detecting, preventing and reporting violations and provide accurate and sufficient documentation of processes and results.