Quality Systems & Policy

Quality Systems

Lark has a structured Quality Management System (QMS) as per the guidelines of WHO-GMP.

Quality Managements System is dedicated to development of process, manufacturing and distribution of products to guarantee safety, efficacy and compliance of customer and government regulations. It comprises of resource management, employee training, quality and compliance data trending and Annual Product Quality Review (APQR) through well-equipped Quality Control laboratories at the site. QMS defines Mankind’s quality responsibility to ensure the achievement of adopted quality standards.

Total Quality Management is committed to customer satisfaction through an integrated system of tools, techniques, and training. It involves continual improvement of organizational processes resulting in high quality products and services.

Corporate Quality Assurance team regularly updates site as per the requirement for continual improvement. It reviews the effectiveness of site quality and contract manufacturing sites according to WHO-GMP compliance. Reviews are carried out for failure, rejection, market complaints, incidents, non-compliance and product stability.

Our Key Quality system includes:

• Regulatory
• IPR
• Clinical
• RnD
• Quality Assurance

Quality control and systems include advanced facility, sophisticated instrument and elaborate microbiology laboratory. Products are tested against the predefined stringent product specification set.

Good Distribution Practices is the Key to delivering products to the patients and consumers. Finished goods storage facilities have adequate controls as per product storage requirement and security.

Quality Policy

To Manufacture :   World-class pharmaceutical formulations.

To Satisfy :   Needs and expectations of customers.

To Ensure :   Employee involvement.

To Build :   Quality at each and every level.

To Assure :   Commitment to safety.

To Invest In :   Continuous improvement.