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Name
Amila Djulovic, MPharm
Title
Regulatory Affairs Specialist - Study Start up and Regulatory
Bio
Amila brings nearly a decade of diverse experience in regulatory affairs to her role. Her expertise spans across Marketing Authorizations (MAs) and Clinical Trials, with a particular focus on GMO-related studies conducted across multiple EU countries. Navigating the regulatory landscapes of both EU and non-EU countries across various regulatory domains has been instrumental in the cultivation of her professional proficiency and expertise in the field.
