Watch this on demand webinar to explore what it means when regulatory authorities require a clinical trial sponsor to maintain the Trial Master File in a state of “inspection readiness”.

Watch this on demand webinar to explore what it means when regulatory authorities require a clinical trial sponsor to maintain the Trial Master File in a state of “inspection readiness”.
Discover how evolving beyond paper-based processes and adopting an eTMF help ensure inspection readiness.
To support manufacturers on the road to the MDR compliance, we have answered some of the most common questions related to it.
Discover the answers to the questions from the Q&A session of our webinar on Agatha, Content Management tool for Life Sciences.
Watch our free webinar about how Agatha helps organisations to optimise the management of their quality and clinical documentation.