(1) Our priority is to respect the environment and human health and to provide safer drug delivery systems.
(2) Our regulatory affairs specialists will be tailored to your specific project to help you cope with an increasingly complex and changing regulatory environment.
(3) We can provide guidance at all stages of your drug development, including customer support and providing all necessary information as needed.
(4) We follow all the below regulations and take them as the premise of all our activities: ISO 15378:2017, ISO 14001, ISO 13485:2014, GMP 2010, YBB.