Petra Kolenc

• translational studies: drug development, preclinical studies, formulation development, writing documentation for first-in-man clinical trials (IMPD, IB, clinical study protocol, ICF)
• planning, organizing, conducting and leading national and European research projects in the field of radiopharmacy and nuclear medicine
• coordinating academic clinical trials
• cooperation in the setting up guidelines for hospital radiopharmacy practice at national and European level (EANM, IAEA)
• organizing scientific events (ESRR), chairing sessions at international congresses, invited speaker at national and international events
• process validation, validation of analytical methods, premises and equipment validation

• quality assurance, documentation management and the release of radiopharmaceutical products, pharmacovigilance
• implementation of new radiopharmaceuticals, process validation

• preparation and quality control of radiopharmaceuticals