Regulatory & Clinical Evaluation
Ra’na has a degree in Biotechnology Engineering from VTU in India.
Prior to working for Qserve, Ra’na was Regulatory Affairs Manager with Philips responsible for regulatory compliance and registration of OTC/active devices.
She has more than 6 years of experience with extensive knowledge and expertise in RA/QA and Clinical Affairs.
She also has experience with Worldwide Submissions over various jurisdictions and
is trained in ICH GCP and has also previously worked with Quintiles.
Her main expertise is in Risk Management according to ISO 14971, Post Market Surveillance and Vigilance.
Learn more about our services within Regulatory Affairs & Clinical Affairs.