The Impact of Disruptive Change in the Clinical Trials Industry on Research Sites
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Target Audience:
- CRCs
- CRAs
- Auditors
- Project Managers
- Regulatory Affairs/Compliance
- Data Managers (Site, Sponsor, CRO)
- Quality Assurance
- Clinical Research Administrators
Program Description:
As we head towards the end of the second decade of the twenty first century a great deal has changed about the way research is done at the site level particularly as it relates to the many disruptive technology driven changes that have evolved. Or has it? After 13 years managing sites and taking the investigator view followed by 13 years in the CRO industry taking the sponsor view, the author will look at what has changed in over a quarter of century and the future holds for clinical research sites. In particular he will look at the site landscape through the lens of four , supposedly major, disruptive changes
Speakers:
- G. Paul Evans, MD, President & CEO, Velocity Clinical Research
Registration Fees:
- Chapter Members: $0
- ACRP Members: $15
- Non-Members: $30
Contact Hour Fees:
- Chapter Members: $0
- ACRP Members: $15
- Non-Members: $30
* Please Note: If you are looking to recieve Contact Hours for this event, you will have to pay both the Registration Fee and Contact Hour Fee.
Contact Hours: 1.5 Contact Hours
Refund/Cancellation: No refunds.