DTA works closely with the Federal Drug Administration (FDA) and Health Canada on your behalf to educate these government agencies on ways to streamline processes to get dental products approved for the marketplace. By providing real-world solutions and resources for our member companies, members are better prepared to tackle the maze of 510(k) submissions, (European Union CE Marks) UDI, and paperwork for exports. Get answers to your domestic and international regulatory questions with the help of FDA consultants (including current DTA members) who work closely with the DTA. Keep up to date on regulatory laws and procedures with our quarterly Regulatory E-Newsletter.
DTA also holds webinars and workshops to help assist member companies with their regulatory needs. For specific regulatory assistance, please contact the DTA at 703-379-7755.