Our Capabilities
Manufacturing
A State of the art manufacturing Facility
Purex Pharmaceuticals CGMP manufacturing plants. Its Active Pharmaceutical Ingredient and intermediates manufacturing facilities established close to the city of Hyderabad and Vishakhapatnam, are capable of handling complex and hazardous reactions. The manufacturing facilities comply with all Regulatory guidelines and requirements of current Good Manufacturing Practices (cGMP)
Research & Development
Purex pharmaceuticals is one of the leading research driven manufacturing facility having focus towards the development and manufacturing of Active Pharmaceutical Ingredients (APIs) and Drug intermediates .
Our R&D team focuses on process development and optimization.
The R&D team of Purex is having 37+ highly experienced, skilled professional scientists comprising doctorates, post graduates and graduates specializing in process & analytical development for the manufacturing APIs and drug intermediates.
There are Kilo & Pilot Labs which are fully equipped with 10L – 200L Glass assemblies for feasibility trials. Our Kilo and Pilot plant are operating in cGMP condition and are capable to scale up process and filing processes developed in the synthetic lab.
Quality
We are committed to the highest standards of quality within our operations. Our Quality division is responsible for ensuring that products are compliant, meets and exceed regulatory requirements.
At Purex pharmaceuticals, our Quality systems are based on GMP ICH Q7A guide and we are committing to continuous improvement in all aspects of our business.
Our Quality Assurance( QA ) department also works closely with our clients and the Health Agencies to ensure that their compliance requirements are meeting expectations. From raw materials to finished products, our Quality Control team conducts rigorous testing and analysis to ensure that every batch of our products meets the highest standards of purity and potency.