Greater San Antonio Chapter: ISO 14155 and FDA Requirements-Trials Conducted at the Research Site (ACRP Webinar Replay)
This event will be presenting a webinar replay from the ACRP Conference Library.
Event Description:
Join us for a webinar replay of a session providing information on FDA regulations and ISO requirements along with the similarities and differences for device trials conducted at the research site.
Speaker:
Pranali Wandile, MS, CCRP, Clinical Research Manager, South Carolina Clinical Research LLC
Learning Objectives:
- Define what is considered a medical device.
- Define and provide examples of an investigational medical device.
- FDA regulations and ISO requirements for device trials conducted at the research site.
Registration & Contact Hour Information:
Registration Cost: $0 (free for all to attend). Please register for this event by 3/14/24.
Contact Hours: This event will offer 1 contact hour. Please claim your contact hours by 4/21/24.
Click here to register and purchase your contact hours.
- Chapter Members (registration only): $0
- Chapter Members (registration + contact hours): $15
- ACRP Members (registration only): $0
- ACRP Members (registration + contact hours): $15
- Non-Members (registration only): $0
- Non-Members (registration + contact hours): $30
To receive contact hours: Purchase the contact hours and attend the program. After attending the event, log on to the ACRP website and visit learning.acrpnet.org, click “GO TO MY COURSE”. Select your event, confirm attendance and take the event evaluation between 1 and 30 days following the event and obtain the online certificate." After 30 days, contact hours are no longer available