Quality at Albinis is clearly demonstrated in all phases of the product lifecycle. Quality supervision begins at the test facilities with careful documentation and general conduct of non-clinical safety studies. This ensures compliance with current Good Laboratory Practice (GLP) and consequently, the integrity of the data produced. Quality supervision then follows through clinical trials, production and distribution, and concludes with shelf-life surveillance.
Albinis Biotech Pvt. Ltd. Our clinical Quality Management System encompasses clinical research documents, activities and information management systems.
Moreover, Albinis ensures that quality is a main concern, investigators and contractors who collaborate with us at the clinical stage.
Albinis has state of the art manufacturing facilities and uses the most advanced testing equipment, to guarantee the quality of our products. Albinis additionally supervises suppliers' procedures in order to ensure that the highest quality materials are used in our products. Once a product gains regulatory approval and enters routine manufacturing, quality is guaranteed throughout the process, for both drug substances and drug products..
Manufacturing processes are validated and equipment is tested and certified test methods are confirmed to ensure that each product is of reproducible quality Continuous improvement practices are employed so that processes and procedures are continually updated Our clinical Quality Management System encompasses clinical research documents, activities and information management systems. Moreover, Albinis ensures that quality is a main concern,
