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”.
Regulated Document Management
eTMF – Your Key to Inspection Readiness
Discover how evolving beyond paper-based processes and adopting an eTMF help ensure inspection readiness.
Medical Device Regulation (MDR): Frequently Asked Questions
To support manufacturers on the road to the MDR compliance, we have answered some of the most common questions related to it.
Webinar Q&A | Agatha – Quality and Content Management Solution
Discover the answers to the questions from the Q&A session of our webinar on Agatha, Content Management tool for Life Sciences.
On Demand Webinar | Agatha – Quality and Content Management Solution
Watch our free webinar about how Agatha helps organisations to optimise the management of their quality and clinical documentation.
