The course will drive you through the nonclinical development  program of a medicinal product, the different studies needed and the International guidelines supporting these requirements.

The course faculty consists of highly experienced experts in the field, Regulators and from Industry.

The course  format includes formal lectures and case studies to discuss in small groups and subsequently present.

A final exam occurs on friday 31st  January, early afternoon.

A home assignment is provided as requested for those students wanting a full grade for the module as part of SafeScimet master. Students will receive it, with instructions for preparation and submission deadlines.

All students will receive a certificate of participation

Those students who fill the exam and the home assignment and pass will receive a Diploma