According to recent research, 70% of adverse events reported across clinical trials are preventable. Of these, more than 60% are caused by technical errors and 17% by inappropriate diagnosis. In C> trials, additional sources of quality risks include:
- Failure to follow an investigational plan (51%)
- Inadequate and inaccurate records (33%), with special reference to chains of custody and identity
In the study, it was clear that these failures are a result of a lack of training and experience of clinical delivery teams. Researchers recommended that C> operational education should not be restricted to a specific protocol but encompass the entire lifecycle delivered through a training platform that provides real-time safety updates, new risk profiles, and scientific advances, to empower research teams throughout product development and manufacturing.
C> manufacturing companies need to develop a dynamic training program that aligns with the on-the-job needs of their employees. It must be delivered in a way that enables self-learning, continuous on-the-job training, periodic performance assessments, and ongoing additions to the curriculum. But how can C> manufacturers customize training programs, understand the skills needed, identify gaps, deliver, and keep track of all the training? They need the right technology.
In this whitepaper we talk about:
- The rising talent gap in CAGT industry
- Key areas where upskilling is critical
- How ComplianceQuest’s training management software can help in upskilling
- And more