Topic 1 – The importance and reasons to conduct clinical trials and what comes before clinical trials
Topic 2 – Common Myths about clinical trials answered
Topic 3- Understanding the different types of clinical evidence required in clinical trials (e.g with NICE, Integrated Care Systems, etc) and the importance of the procurement process
Topic 4: The importance of protocols and adhering to them including CE Marketing & the Upcoming (Brexit) Changes
Topic 5- The importance of clear data management principles (e.g. Device Master Records)
How to join: There is no charge to attend this course: simply register at www.masteringclinicaltrials.org.
Once registered, you will be given access to information about our virtual platform.