Quality Management System

Quality Management System

  • We are commited to produce Drug Product with Highest Quality ,Safety and Efficacy for customer Satisfaction.
  • Continuous Improvement is inculcated in to our Quality Management System.
  • We are also Committed to meet national and international standards in accordance with statutory and regulatory requirement in producing consistent Quality of Drug Product .
Our quality chain system covers three key functional areas

Quality Assurance (QA)

Quality assurance comprises of Corporate QA and Site QA. Site QA is responsible for implementation of quality systems throughout the organization. It is also responsible for all audits including regulatory, customer, GMP, WHO, good laboratory practices and good documentation.

Quality Control (QC)

Highest quality standards are the key driver of success for any company. Effective quality control procedures are being carried out at different levels to maintain high standards. Quality control is responsible for all chemical analysis. It also acts as a support during product development and validations. QC is supported by an experienced and qualified team of professionals.

Regulatory Affairs (RA)

Regulatory Affairs ensures compliance with the requirements of national and international authorities. This helps us to ensure that our products meet the required standards. Our regulatory affairs team develops regulatory strategy and integrates legal constraints into product development plans. Moreover department ensures that the firm adheres to the laws protecting public health.