2021 Ensuring Safe Medical Device Use: FDA’s Role in Product Regulation, Your Role as a Device User
June 2, 2021
OBJECTIVES: Upon completion of this activity, the participant should be able to:
- Review the premarket regulatory processes used by FDA to provide reasonable assurance of the safety and effectiveness of medical devices
- Present the FDA resources available to facilitate the safe use of medical devices by surgeons, and their important role in voluntary reporting
ACCREDITATION: The A. Webb Roberts Center for Continuing Medical Education of Baylor Scott & White Health is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
DESIGNATION: The A. Webb Roberts Center for Continuing Medical Education of Baylor Scott & White Health designates this live activity for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Meets Texas Requirements for 1 Hour of Ethics/Professional Responsibility Credit
WebEx
Temple, TX
76508
United States
Available Credit
- 1.00 AMA PRA Category 1 Credit™The A. Webb Roberts Center for Continuing Medical Education of Baylor Scott & White Health is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
- 1.00 Ethics
- 1.00 Attendance
- 1.00 Ethics