Given the COVID-19 pandemic, we want to make sure that our programmes can be followed in a safe environment for you. Therefore, we will switch this course to a series of live online sessions (webinars) until further notice. You can register for the course here, as we will ensure that your registration will be transferred to the online format. If there is a price difference you will be invoiced the lower amount.

Do you want to understand more deeply the sponsor co-monitoring practice and how this yield benefits in clinical research? Several sponsors have developed successful co-monitoring strategies, but do we understand how critical this is in terms of not merely CRA oversight but for overall conduct of the clinical trial. This course provides you with the grounding that will allow you to understand the most salient aspects of co-monitoring practise.

During a one-day face-to-face course in which presentations are blended with interactive sessions with the attendees, you will receive a good oversight on regulations guiding co-monitoring, principles of CRA oversight, tools and methodologies, and above all comprehensive guidance how co-monitoring can improve conduct and quality of your clinical trial. The course will present real life case studies and examples where either CRA performance or indeed site performance has not been adequate and will use interactive workshops to find ideal solutions. Exercises for self-assessment are used to enhance your understanding of the main topics discussed in the course. You will be able to test your comprehension with a final grading assessment.