Join our latest webinar on the 1st of June where our first speaker, Susanna Hellström, Consultant Clinical Development will present the role of the monitor in clinical studies. You will get a brief overview of the visits they perform and obstacles they can encounter working with a study.
Kristina Edner, Consultant Clinical Development, will also present the advantages of using an electronic Trial Master File (eTMF) for your clinical studies. The Key2Compliance solution for an eTMF is ISO 14155 compliant for all essential documents collected during clinical studies.
Who should attend?
Manufactures of Medical Device, IVD and Pharma planning to start a clinical study and healthcare professionals performing clinical studies.
Your key takeaways
- The role and duties of a monitor
- The monitor is a support function for the site study team
- The importance of the Trial Master File
- The benefit of an electronic Trial Master File
Date: 1st of June