This chapter contains 5 modules covering; Site Selection for a Trial; Trial Start Up Requirements: From Site Selection to Site Initiation; Trial Active Stage: Managing the Subjects and Monitoring; After Patient Completion: Responsibilities for the data; the documents and reporting results and Trial Master File and Site Files – Design; Management and Archiving. These modules are prepared for health care professionals’ level 2 beyond the basics and are focused on the requirements at the site; prior to a Clinical Trial; right through to the responsibilities following Trial completion.
Expected to reach 3-5 billion by 2020 representing half of the world’s population, Africa’s population offers access to drug naïve patients in multiple disease areas as well as an underrepresented demographic in clinical trials. eMQT is uniquely placed as the bridge between the pharmaceutical, Biotechnology and Technology industries and Africa, utilizing research healthcare experts and technology enabled innovation to provide access to patients, high quality evidence based patient data and ultimately patient access to medicines.
