Quality control is an essential operation of the pharmaceutical industry. Prelims Pharma is committed to better healthcare for all, through quality products, achieved through manufacturing excellence, compliance to requirements and continual improvement in quality management system, for maximum customer satisfaction.
We believe that a solution becomes a success when it conforms to the quality specifications by the customer every time, meeting world-class standards. Prelims Pharma implements an unmatched global quality management system that is based on the desire to sustain a culture of operational excellence. Prelims Pharma employs the best of industry’s technical officials in its QC, QA, and production and product development department. Their continuous proactive efforts on the present and future needs of market are dedicated to meeting the customer requirements through consistent development of technology, quality, drug delivery systems, and packaging. Our company’s passion for quality goes way beyond business and statutory requirements.
Quality Assurance
Quality assurance department, a fully autonomous functionality is in place to keep track of each activity, parameters & processes to achieve the quality goal in totality. Quality of each medicinal product is assured by applying TQM techniques by the QA-Team. Quality assurance is a wide concept that covers all aspects that collectively or individually impact the quality of the product. That is, the sum of organized arrangements that are made with the aim of ensuring pharmaceutical products are of the required quality as per the intended use. Quality assurance is a good practice in the manufacture of pharmaceutical products, as it is the process of vouching for integrity of products to meet the standard for the proposed use. It is an obligation that ensures manufacturers meet the needs of end-user needs in terms of safety, quality, efficacy, strength, reliability and durability.
Objectives of Quality Assurance
- To ensure the law is complied with to the latter.
- To offer protection of the manufacturing organization.
- To offer a guarantee that the person who is administering medicine is confident that every unit will achieve the desired effect.
- To protect users for products from possible accidental defect in the manufacture, design, storage as well as usage instructions.