Therapiva is committed to providing high quality products to the customers and to meet this commitment, it has implemented current good manufacturing practices across the manufacturing site, encompassing all areas of business processes right from supply chain to product delivery. This enables to maintain consistent quality, efficiency and product safety.
The quality management systems applicable to chemical and process development, analytical development and testing, contract research and development, and manufacture of pharmaceutical products, have been certified by NVT Quality certification to be in compliance with ISO 9001:2015 until June 2020. The Department of Drugs Control Administration, Hyderabad, Government of Telangana, has certified that the facilities conform to good manufacturing practices. The goal is to attain compliance and certifications for USFDA by 2020.
The internal audit procedures are also regularly updated to comply with any changes in international regulatory requirements, such as US FDA, PMDA etc..