This 6 Module course provides a thorough introduction to medicines development in approximately 12 hours of study.
The text is drawn from the Base Text and is supplemented by narrated slides and multiple choice questions with answers.
The course can be combined optionally with the Base Case and e-Tools , with links provided to the relevant sections, to become a deep practical learning experience.
Details of the 6 Modules and their contents are described below.
The course consists of the following 6 modules:
Module 1: Overview of development
Module 2: Screening and nonclinical development
Module 3: Introduction to clinical development
Module 4: Phase I and Phase IIA/Proof of Concept
Module 5: Phase IIB and III studies and pharmacoeconomics
Module 6: Filing for regulatory approval, marketing and recap of the development process
A certificate of completion is available on certifying that the materials have been followed for each module and passing a mutiple choice examination.
Further information is available through the Contact form.