Åsa Kjellström joins SDS!
We are happy to welcome Åsa Kjellström, PhD, who will extend the Drug Development team as a Senior Advisor Regulatory Affairs and Clinical Development. Prior to joining SDS, Åsa was working as a Clinical assessor at the Swedish Medical Products Agency, MPA. At MPA she focused on safety and efficacy evaluation of new medicinal products as well as safety surveillance of approved drugs. Her previous experience also includes over 15 years in the pharmaceutical industry at SOBI and AstraZeneca within the fields of nonclinical, drug safety and regulatory affairs. Her competence is a perfect fit for our clients in clinical development.