Zenara offers a versatile formulation development and manufacturing facility for solid oral dosage forms, located in Hyderabad, India. The facility is EU GMP accredited and employs stringent cGMP quality and regulatory systems
Zenara has an unwavering commitment to quality. We welcome our clients’ audits of our quality systems. These audits form the basis of our quality systems that are critical to our successful inspections by worldwide regulatory agencies.
Our quality and regulatory affairs specialists are actively involved in overseeing conformance with customer and government requirements during each step of the process. This experience and oversight is central in ensuring that products are manufactured to meet strict cGMP requirements and customer defined specifications.