Ind – Swift is committed to improve life of people by providing quality medicine. Ind –Swift 's management, through corporate quality assurance, fully supports a formal and continuing program of preview, evaluation and modification of operations at all levels. To ensure the consistent quality of the product & to continuously meet the customer's requirements, we have stringent Quality Assurance Systems in place for monitoring and upholding the over all quality system. The control of the product quality during production is maintained by in-process quality tests and quality audits. A continuing employee training program, equipment and process validation and a self-inspection program are part of the company’s approach to Quality Assurance. Special emphasis is placed on thorough documentation (SOPs, Master Formulae, Specifications, Validation Protocols etc.) and review of the entire manufacturing and control process. Our Quality Assurance systems are supported by our Quality Policy and Quality Manual, which have been compiled as per cGMP Directives and Guidelines and the directives of various international regulatory bodies like the USFDA, UKMHRA and the EC.


Quality Assurance is headed by Vice President – Quality Assurance & Regulatory Affairs, who has vast experience of 24 years in Quality Control and Quality Assurance functions in pharmaceutical formulation plants of repute.

There are approved standard operating procedures for each and every activity carried out at the site. Implementation of these procedures is the responsibility of the user, which is monitored by a team of trained Quality Assurance executives/officers. Manager - Quality Assurance approves all the procedures, protocols and reports. For each product, in-process specifications, finished product specifications, analytical procedures and limits are defined and checked by Manager - Quality Assurance . Approved specifications for raw materials and packaging materials are also available to control the quality of inputs going into the products.

 
 
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