Quality Control

Quality is a relentless policy at Psychotropics India Limited & managemnet is always desirous to provide the customer desired quality medicines at competitive cost & maintain leadership in healthcare through continual improvement & innovative technology. Quality control is an essential operation of the pharmaceutical industry. We are very conscious of the fact that our drugs are prescribed by the reputed doctors of the country & hence they should be safe and therapeutically active formulations whose performance is consistent and predictable. We at Psychotropics are committed to provide excellent quality products. Despite other factors, one major reason for our success today is that we have never compromised with the Quality. We have strived hard from last 20 years to keep on manufacturing good quality products to ensure that the patients get healthy & stay more active lives. Stringent quality control and continuous quality checks are a part of every batch and process at Psychotropics and is a part of our long-term approach, adding value to our quality competence.

Our Quality Control Laboratory comprises of the most modern equipments like HPLC, FTIR, UV, GLC, IR etc. The SOP’s for our quality system are well defined. We have different laboratories for Instrument, Chemical & Microbiology testing in every manufacturing location. At the same time we are always looking for more exacting and sophisticated analytical methods that can be developed for their evaluation.

Quality Assurance

The QA department is instrumental in preparation of protocols, Sop’s and monitoring qualifications, strict process control; process validations; stability studies; training and development; self-inspection and audits; systems and procedures and relevant documentation. The role of QA is critical in ensuring that the medicines manufactured are of top quality. We at Psychotropics have 2 Quality Assurance departments within every manufacturing location to safeguard the quality of our products. The 1st QA department works very closely with the production department to ensure that no mistake is carried at the time of manufacturing which would eventually result in any quality related issue. It is therefore instrumental in preparation of various SOPs related to the production, testing, release, packaging and labeling of the APIs. It also keeps a check on the entire manufacturing process right from sampling, dispensing, mixing, in process quality control, holding, packing etc. The 2nd QA department we have in Psychotropics is looking after the stability studies & process validation. This department works independently & is not involved in the day to day manufacturing activities of the plant. The role of this department is to carry out the stability studies & prepare the data of the products that are manufactured in the factory. This department has its own independent equipments like HPLC, Stability chambers (both real time & accelerated), UV etc.