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Quality Assurance Department

"Quality Assurance" is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. It is the totality of the arrangements made with the object of ensuring that pharmaceutical products are of the quality required for their intended use. The system of Quality Assurance appropriate to the manufacture of pharmaceutical products should ensure GMP and GLP.

 

Delta Pharma Limited has implemented a comprehensive quality system (ISO 9001:2015). Quality Assurance (QA) procedures ensure that the quality of the products is maintained by strict compliance with international pharmacopoeias (BP, USP, etc) specifications on raw materials, packaging materials and finished products. This department enables implementation, assessment, and reporting which is necessary for guaranteeing that the products manufactured by maintaining cGMP and conform to the requirements and expectations of the customers.

 

The department is responsible for maintaining all documents, records and standard operating procedures (SOP), making sure that they are up to date. We accord highest priority to quality control and adequate precautions are taken to ensure that there are no lapses on this front.

 

As a part of quality assurance, Delta Pharma has a Quality Control Department comprising physical, chemical, instrumental, microbiological sections and equipped with state- of -the-art analytical and microbiological quality control instruments for our quality control at each and every stage of the manufacturing process.