Lisa Lindholm

Lisa Lindholm is a seasoned professional in Regulatory Affairs and Quality Assurance with over 20 years of experience in the pharmaceutical industry. Currently serving as the Head of Regulatory and Quality Affairs at Ipsen since February 2017, Lisa is responsible for strategic decisions and compliance in the Nordic Area. Prior to Ipsen, Lisa held various roles at Actavis (now Allergan), including Executive Director of Regulatory Affairs and Nordic Director of Pharmaceutical Affairs, where responsibilities encompassed Regulatory Affairs, Quality Affairs, and overseeing the Pharmaceutical Affairs Department in the Nordics. Earlier experience includes the role of Nordic Regulatory Affairs Manager at Eisai and Regulatory Affairs Manager at Sandoz. Lisa holds a Master of Science in Pharmacy from Uppsala University.