This seminar offers key market opportunities by enhancing understanding of FDA device regulatory processes, including 510(k), IDE, PMA, HDE, and De Novo applications. It emphasizes pre-submission ...
Medical devices play an essential role in improving the quality of human life. Consequently, their design poses unique engineering challenges. Designers must address high standards of reliability, ...
Market opportunities include providing training and consulting services to medical device companies for FDA and EU MDR compliance, especially in design controls, verification and validation. This can ...
On-demand programs deliver clinically relevant science, technical instruction, and case applications in small animal and equine practice ...
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