Learn how to accelerate your study start-up while maintaining billing compliance, obtaining the required funds for the study, and reducing risk exposure.
Implementing and maintaining effective research administration practices can be difficult for any clinical trials office. Join PFS Clinical for a 1 ½-day workshop to gain valuable insights into all aspects of research administration. This workshop will include speaking sessions by our administration and compliance experts, case studies, and hands-on activities. Topics will include:
Compliance Considerations for Budgets
High-Risk Contract Considerations
Efficient Study Start-Up and Negotiations
Maintaining Compliance Throughout a Study