Quality Management
Quality Management
Quality management is a comprehensive system designed to ensure the consistent safety, efficacy, and quality of drug 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.
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
Welcome to New Alliance Fine Chem Pvt. Ltd.
New Alliance Fine Chem Pvt. Ltd. is the leading manufacturer of premium quality of Chelating Agents, Protein Hydrolysates, Fine Chemical (including Mineral & Metal Salts) & Speciality Chemicals, headquartered in the Mumbai, which is the financial capital of India. We are having two state of art manufacturing facilities in Tarapur MIDC, which is about 100 Km to the north of Mumbai. It is well accessible to the Airport & JNPT Sea Port.
Since 1986, we are supplying our specialty Salts through steady growth to our customers in the different sectors of application like food, nutritional supplement, pharmaceutical, biopharmaceutical, cosmetic and industrial applications around the globe. Our production facilities are ISO 9001:2015, ISO 22000:2018, FSSC 22000, ISO 14001:2015, ISO 45001:2018 and FSSAI certified. The product portfolio includes more than 350 Mineral Salts from organic and inorganic chemistry.
We are a company in search of excellence & continuity. Our manufacturing plants in Tarapur MIDC illustrate these principles. We have refined our processes which helps us to deliver our customer, a customized product.
As our customers are our valued partners, we are dedicated to giving them the finest quality of the product & customer service.
We focus ourselves to work on the strategic application of new ideas and technologies to improve productivity, create new markets, and generate sustainable expansion. We put our full efforts in R&D to have a competitive advantage, to adapt to the needs of our customers & to find new opportunities in the market. R&D is crucial for long-term growth and staying relevant in a rapidly evolving chemical industry.