Claudia Del Amo

I have learned more about the role of regulatory affairs and its different caveats, I am now also able to identify the different regulatory frameworks, authorities and pathways governing the marketing authorisations of different types of medicinal products. One of the most important points is the scientific background needed to understand if the data you are including in a marketing authorization application makes sense. My most positive experience was the fact that the instructors are professionals with great experience in the field, reflects in the way they explain the regulatory concepts. Also, the flexibility to do the course remotely is very helpful. It is a very instructive introductory course which helps to set the foundations of further knowledge that will be acquired along the rest of the STARS programme.