Impact of Covid-19 Pandemic in Clinical Trials: Considerations and Tools
Please click here to purchase your contact hour.
Speakers:
-
Anne Blanchard, CCRA, CEO - Development Strategy and Quality Assurance, Blanchad & Asociados - LATINABA
Target Audience:
- CRCs
- CRAs
- Investigators
- Auditors
- Project Managers
- Regulatory Affairs/Compliance
- Data Managers (Site, Sponsor, CRO)
- Medical Monitor, Medical Officer, Project Physician
- Quality Assurance
- Clinical Research Administrators
- Other
Program Description:
Review how Clinical Trial Implementation is changing for research that was ongoing before COVID-19 Epidemic and how sites and Sponsors must prepare to face this challenging times.
Program Agenda:11:45 AM - Webinar setup
12:00 - 1:00 PM Educational Presentation
Learning Objectives:
- Be able to assess how the present worldwide pandemic is affecting ongoing clinical trials and clinical research professionals
- Be familiar with Key elements of a Risk Mitigation Plan and practical tips that may help in the implementation
- Establish priorities in managing protocols moving forward
- Understand key Regulatory Agencies guidance
Contact hours: 1.0 Contact hours have been applied for through ACRP.
Membership is not required for online registration of contact hours.
To receive contact hours: Purchase the contact hours, sign in at the event, and attend the program. Log on to the ACRP website then “My Courses” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Registration Cost: FREE to all Chapter Members, ACRP Members, Non-Members
Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
Refund Policy: Not applicable