In this 90-minute audio conference you will learn the following:

Working knowledge of good clinical practice (GCP) and regulations regarding human subject protection.  Key to good practice is implementing training and education into your research practice.

Understand the differences between clinical practice and clinical research.

Bringing clinical research to your practice is a big commitment.  Tips on getting  buy-in from all your staff members so they don’t view their added duties as an imposition. 

Who will lead your team as principal investigator?  Guidance on “reading” your interested physicians and garnering their support as sub-investigators.

Understand the practical aspects of conducting clinical trials…how to decide which trials best fit your site’s resources and patient population…and how to evaluate protocols for feasibility.

How to develop a marketing plan to recruit patients.  Without patients/subjects to populate the study, there would be no study.

Guard against ill-prepared sites which incur all start-up costs and not realize the full potential if enrollment falls short.