TAB CDRH is an abbreviated term that stands for "Technical Advisory Board for the Center for Devices and Radiological Health." It refers to a specific board or committee that operates within the U.S. Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH).
The CDRH is responsible for ensuring the safety, effectiveness, and proper regulation of medical devices and radiation-emitting electronic products in the United States. As part of this regulatory process, the CDRH appoints and utilizes the expertise of the Technical Advisory Board (TAB CDRH).
TAB CDRH consists of a group of external industry experts, scientists, clinicians, and other professionals who possess knowledge and experience in various relevant fields, including medical device evaluation, testing, research, manufacturing, and clinical practices. Their expertise assists the FDA in making informed decisions regarding regulatory policies, evaluations, approvals, and other important matters related to medical devices and radiological health.
The TAB CDRH holds regular meetings to review and discuss scientific and technical issues, provide recommendations, and offer expert opinions on various topics related to the CDRH's functions. Their insights and recommendations contribute to the development and refinement of regulatory policies and decisions, aiming to ensure the safety, effectiveness, and proper use of medical devices in healthcare settings.
In summary, TAB CDRH is a technical advisory board that supports and assists the FDA's Center for Devices and Radiological Health in making informed decisions and recommendations related to the regulation and safety of medical devices and radiological health in the United States.
