Quality Policy
Quality Is Our Priority. Excellence Is Our Commitment.
At Psychotropics India Limited (PIL), quality is at the heart of everything we do. Through rigorous product testing, effective quality assurance systems and adherence to regulatory requirements, we strive to maintain consistent quality across our manufacturing operations and support our commitment to healthcare excellence.
Product Testing
& Analysis
Quality Manufacturing
Practices
Three Pillars of Quality
PIL’s quality chain covers three key areas in each plant, supported by good manufacturing, laboratory and documentation practices to ensure consistent product quality.
Quality Control (QC)
Responsible for testing products using validated analytical and testing methods to ensure that finished products meet all specifications. It also supports validation and qualification processes.
Quality Assurance (QA)
Responsible for implementing and harmonising systems throughout the group companies, conducting audits, organising internal training programmes, approving vendors and managing stability study programmes.
Regulatory Affairs
Responsible for establishing procedures relating to the requirements of domestic and international regulatory authorities.
Our Commitment to Quality and Excellence
At Psychotropics India Limited (PIL), quality is at the core of everything we do. Through good manufacturing, laboratory and documentation practices, we focus on maintaining consistent product quality. Our quality framework brings together product testing, quality assurance and regulatory procedures to support our commitment to healthcare excellence.
Our Quality Assurance Framework
Our quality framework brings together three key areas — Quality Control, Quality Assurance and Regulatory Affairs. These functions work together through validated testing methods, quality systems, audits and regulatory procedures to support consistent product quality.
Quality Control is responsible for testing products using validated analytical and testing methods to ensure that finished products meet all specifications. It also supports validation and qualification processes.
Quality Assurance oversees the implementation and harmonisation of systems across group companies. Its responsibilities include audits, internal training programmes, vendor approvals and stability study programmes.
Regulatory Affairs is responsible for establishing procedures relating to the requirements of domestic and international regulatory authorities.
PIL follows good manufacturing practices as part of its approach to maintaining consistent product quality. Its manufacturing facilities are described on the official website as WHO GMP certified.
PIL’s laboratories are equipped with instruments including HPLC, FTIR, Gas Chromatograph, Auto Samplers and Titrator. The company also lists stability chambers in accordance with ICH guidelines.
PIL identifies good laboratory and documentation practices as part of the practices that support consistent product quality. Quality systems are implemented and harmonised across group companies.
PIL’s Quality Control function supports validation and qualification processes, while Quality Assurance is responsible for stability study programmes. These activities form part of the company’s published quality framework.