Minnesota Chapter: Research Is As Research Does: Does Drug or Device Experience Really Matter?
Please Click Here to Purchase your Contact Hours Target Audience:
- CRCs
- CRAs
- Auditors
- Project Managers
- Regulatory Affairs/Compliance
- Data Managers (Site, Sponsor, CRO)
- Quality Assurance
- Clinical Research Administrators
Program Description:
This session will explore the difficulty clinical research professionals face when either presented with an opportunity to cross over from drug to device studies and vice versa, or a sponsor takes the leap of faith and hires a professional to a device (or drug) company when they have several years of drug (or device) experience and no years of device (or drug) experience. As a result of this continued practice, we are creating unnecessary barriers to grow our teams and our careers. The regulations may be different, but our skill sets and strengths are all the same.
Speaker:
- Lisa Haney, Sr Clinical Quality Specialist, Medtronic
Registration Fees:
- Chapter Members: $0
- ACRP Members: $15
- Non-Members: $25
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 Contact Hour
Refund/Cancellation: No refunds.