Quality Management
Quality Management
Quality management is a comprehensive system designed to ensure the consistent safety, efficacy, and quality of products through a structured framework of policies, procedures, and processes. It includes activities like Quality Assurance (QA), Quality Control (QC), and Risk Management to ensure compliance with strict regulations, such as Good Manufacturing Practices (GMP), and to drive continuous improvement throughout the product’s lifecycle.
We practice Total Quality Management (TQM), which incorporates a zero-defects approach to achieve the highest standards of quality. We ensure conformance to customer requirements through our robust quality management system (QMS) by following the procedures as below.
Policies and Procedures
These are formalized documents that outline how quality will be achieved and maintained.
Documentation
Thorough and accurate documentation is essential for traceability, accountability, and compliance.
Risk Management
This involves systematically identifying, assessing, and controlling risks that could impact Production Processes & Product Quality.
Quality Control (QC)
Measures taken to prevent errors and defects in products by monitoring and testing at various stages.
Quality Assurance (QA)
A broader system of activities that guarantees products are safe and effective by ensuring compliance with standards.
Change Control:
A systematic process for evaluating and managing changes to prevent negative impacts on product quality.
Deviation Management
Procedures for handling deviations from standard operating procedures, including root cause analysis and corrective actions.
Corrective and Preventive Actions (CAPA)
Systems to address existing quality issues and prevent potential ones from occurring.
Validation
Ensuring that processes, systems, and equipment consistently produce predetermined results.
Training
Ensuring all employees are knowledgeable about quality-related procedures to minimize errors.
Audits and Monitoring
Regular internal and external audits and ongoing monitoring to ensure compliance and identify areas for improvement.
Purpose and Importance
Quality assurance (QA) ensures that the finished products are safe, reliable, and meet regulatory standards by implementing processes and standards throughout the production cycle. Its importance lies in reducing defects, improving efficiency, and ensuring product consistency, which builds customer trust and brand reputation, prevents costly recalls, and avoids Product rejection & recall, ultimately making operations more profitable and safer.
We are dedicated to providing high-quality products, trusted by leading companies in Pharmaceutical, Food & Beverages, Dairy Industry, Veterinary, Agriculture, etc. Our top priority is ensuring ingredient safety and quality at every step.
We follow a strict and well-organized Quality Management and Assurance System to deliver consistent and reliable ingredients that meet customer expectations.
To maintain high standards, we regularly monitor and update our quality control processes based on the latest national and international certifications.
We strictly follow all required national and international certification standards, including ISO 9001:2015, ISO 22000:2015, ISO 14001:2015, ISO 45001:2018, FSSC, FSSAI, KOSHER, and HALAL. These certifications are carefully implemented and maintained through regular audits, inspections, and rigorous quality control and assurance systems.
Our advanced Quality Control (QC) lab is built to global standards, ensuring that every product meets the highest levels of safety and quality.
We are focussed on continuous improvement by upgrading our quality certifications, production processes, and assurance systems. This helps us provide safe, pure, and standardized ingredients to our customers worldwide.
Consistent high quality products are manufactured with strict adherence to GMP and GLP.
Quality management operations begins before purchase of raw materials.
High quality of raw materials is ensured by regular vendor audits.
A testing chemical laboratory takes care of purity of raw materials and also verifies that impurities are within desired limits.
Production is carried out under supervision of experienced qualified staff. This ensures that output is proper in all aspects.
In-process testing is carried out to ensure that manufacturing activity is proceeding in right direction.
Finished products are tested for purity and impurities.
In-house microbiological testing facility is to ensure that products are not containing pathogens. This ensures that products are suitable for human consumption.
Compliance with various guidelines is ensured under the presence of robust Quality Management System (QMS). We are committed to follow the procedures & practices as per the statutory & regulatory requirements as applicable. We encourage teamwork & create quality awareness amongst our work force for enhancing our skills.
Quality Management system plays a key role in our production activity.
At New Alliance Fine Chem Pvt. Ltd, consistent quality through compliance with Quality systems and on-going research and development are top priorities.