Building in quality can lead to transformational process changes
A well-known cliché advises that if you fail to plan, you are planning to fail. When it comes to study startup these words ring true, especially as the clinical trials sector is making strides in boosting study quality. With the help of leading practice guides, tools, templates, and automated workflows for study startup, Sponsors and CROs can proactively plan. These stakeholders can agree on and document key elements that can drive quality, efficiency, and compliance while reducing risk and cycle time. These elements enable organizations to document decisions and operational practices to allow sponsors to use a more balanced approach for CRO oversight, and allow CROs the autonomy to effectively meet and exceed sponsor requirements. This proactive approach is becoming essential to enabling parties to constantly be audit-ready, and to increase the likelihood of positive regulatory inspection outcomes.
Getting it right from the beginning — prior to site activation — is key. Too often, these issues are not addressed upfront, resulting in inefficiencies and problems that are not identified until much later, when the study is already underway. Reversing this trend means building in quality from the start. This approach aligns with regulatory initiatives to manage risk, leading to improved study quality.
In this webinar, co-presented with the Avoca Quality Consortium, leading practices for proactive study startup planning will be shared. Participants will learn how to effectively deliver on improved overall study quality while supporting regulatory compliance for provider oversight.
In this webinar, we will explore:
This webinar is applicable to: