3rd European Clinical Trials Inspection Readiness Summit
May 22 - 23, 2017 - Harlington, Hayes NY US3rd European Clinical Trials Inspection Readiness Summit
cventurina@exlevents.com
Phone:+1 212-400-6240
The 3rd European Clinical Trials Inspection Readiness Summit is designed to explore best practices for developing and maintaining compliance at clinical trial inspection sites. Delegates will leave the event armed with strategies regarding partner oversight, metrics, data quality, TMFs and risk assessment tools. Additionally, this event will provide opportunities for sharing best practices and networking across all contributors and stakeholders, including sponsors, regulators, CROs and project teams. Top 5 Reasons to Attend for 2017: 1. Review crucial information and analyze regulations from around the world, with a focus on FDA, EMA, PMDA and MHRA regulations 2.Benchmark the success of your clinical trial using metrics that measure the performance of CROs and trial sites 3. Learn strategies for ensuring there is a comprehensive clinical trial storyboard so inspectors can recreate the trial 4. Leverage process maps that can be applied to streamline TMF management and the key team members who need to be involved 5. Innovate your inspection readiness SOPs to arm them with information on risk-based modeling for inspection readiness