Quality Assurance Department

Quality Assurance is a wide ranging concept which covers all matters which individually or collectively influence the quality of a product. It is the total sum of the organised arrangements made with the object of ensuring that medicinal products are of the quality required for the intended use

The Goal of Quality Assurance is to deliver product of un-compromised quality by implementing stringent quality procedures and controls on the entire product life cycle from development to shelf life.

We adopted a policy of operating the pharmaceutical manufacturing under control of Quality Management System which includes

Change Control System
Deviations Handling
Incidents & Failure Investigations
Out Of Specifications (OOS)
Customer Complaints Handling
Product Quality Review
Recall & Returned Goods Handling
Corrective & Preventive Actions (CAPA)
Quality Risk Management (QRM)

Validation and Qualification is an integral part of quality assurance, associated with every product, system and process which includes

Validation Master Plan (VMP)
Equipment Qualification
Process validation
Cleaning Validation
Method Validation
Vendor Qualification