LLS's Global standard manufacturing plant of general tablets, capsules & semi-solids at Akola by design ensures compliance with regulatory expectations as established by global agencies. The plant is WHO-GMP & EU-GMP certied.

The state-of-the-art facility uses advanced technology to manufacture quality medicines. A separate pilot area ensures the development and scale-up of simple to complex formulations. The manufacturing facility possesses capabilities to manufacture complex formulations developed in R&D with innovative technologies to make them accessible to the masses. All critical Quality Control instruments use modern technology to provide accurate results while remaining compliant with regulatory requirements.

While upholding quality, Leben continuously strives to rationalize the cost of manufacturing to ensure that they are manufactured & made available to patients at reasonable costs. With the consistent quality, the trust of patients and healthcare professionals in our products has strengthened over the years.