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