We are committed to manufacture quality health care products through Good Manufacturing Practices to emerge as a growing force in the Pharmaceutical Market. Company will achieve this through a process of continuous quality improvement. It is our policy to continually meet and exceed customer's needs, the only way to ensure Company's growth and prosperity.
We are committed to improve and upgrade our quality standards to meet the national and international quality requirements through advanced production methodologies available.
This policy will be translated into producing products of high quality at our work place through emphasis on creating strong awareness among the employees, through training and motivation.
The list of our quality policy
- Good manufacturing practices with compliance to cGMP
- Building quality into our products at all levels
- Involvement of all employees
- Continuous quality improvement
- Sensitivity towards environment
QA & Regulatory Affairs
- Q.A. and Regulatory Affairs team comprises of a wealth of experience in all areas of cGMP implementation, audits and compliance, Regulatory Dossier preparation, submission, deficiency response, updation to regulatory agencies and customers.
Research & Development
- We have Highly qualified and experienced scientific team and independent laboratories for chemical synthesis development and analytical method development and validations.
- Creating a product pipeline through Research and Development
The company consistently develops non patent infringing processes to expand its pipeline of products. We have begun our manufacturing journey with generic products at our R&D labs and R&D team is actively seeking to come up with processes that will enable us to manufacture and market generic versions of products.