Quality Control Policy

At Sharing Formulations Pvt Ltd, we are committed to delivering products of the highest quality to meet the healthcare needs of our customers. Our Quality Control Policy reflects our dedication to maintaining rigorous standards, ensuring the safety, efficacy, and reliability of our pharmaceutical products.

• Compliance with Regulatory Standards: We adhere to all relevant local and international regulations and guidelines, including those set forth by the Food and Drug Administration (FDA) and other regulatory bodies. We continuously monitor and update our processes and procedures to stay in compliance with evolving regulations.
• Quality Management System: We have implemented a robust Quality Management System (QMS) that encompasses all aspects of our operations, from raw material sourcing to manufacturing, packaging, and distribution. Our QMS is designed to promote quality at every stage of the product lifecycle and is regularly reviewed and audited to identify areas for improvement.
• Qualified Personnel: We employ a team of highly skilled and trained professionals who are committed to upholding our quality standards. Our employees undergo regular training to enhance their knowledge and skills in areas such as Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and quality control techniques.
• Raw Material Evaluation: We meticulously evaluate and select suppliers based on their ability to provide high-quality raw materials. All incoming raw materials undergo rigorous quality checks to ensure they meet our specified standards for purity, potency, and safety.
• Robust Testing and Analysis: We conduct comprehensive testing and analysis at various stages of the manufacturing process. This includes in-process testing, stability testing, and final product testing to verify the identity, potency, and purity of our formulations. We utilize advanced analytical techniques and equipment to ensure accurate and reliable results.
• Documentation and Record-Keeping: We maintain thorough documentation and record-keeping practices to track and document all activities related to quality control. This includes batch records, laboratory reports, and other relevant documents. These records enable us to trace and investigate any quality-related issues and facilitate product recalls if necessary.
• Continuous Process Improvement: We foster a culture of continuous improvement by regularly reviewing and analyzing our processes and procedures. We encourage feedback from employees, customers, and stakeholders to identify opportunities for enhancement and implement corrective actions when needed.
• Supplier and Vendor Management: We establish strong relationships with our suppliers and vendors based on mutual trust and collaboration. We evaluate their quality systems, conduct regular audits, and ensure that they meet our stringent quality requirements. We work closely with them to address any quality concerns promptly.
• Adverse Event Monitoring and Reporting: We have established mechanisms to monitor and track any adverse events or product complaints. We promptly investigate and address these issues, ensuring that appropriate corrective and preventive actions are implemented to prevent recurrence.
• Customer Focus: We prioritize customer satisfaction by providing products that meet or exceed their expectations. We actively seek customer feedback and take it into consideration for continuous improvement.

This Quality Control Policy is communicated throughout the organization to ensure that every employee understands their role in maintaining and enhancing the quality of our products. We are committed to upholding the highest standards of quality control to safeguard the health and well-being of our customers and to maintain our position as a trusted pharmaceutical company in the industry.