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Medical Device Academy, Inc. can help you with your medical device regulatory submissions. We specialize in 510k submissions, preparation of CE Marking Technical Files and Canadian device license submissions. We also created a new business unit that specializes in preparing, printing, validating and shipping FDA eCopies for 510k pre-submissions, 510k submissions and De Novo applications. Most of our clients are small and mid-size medical device companies that need continuing education training, and quality System Auditing for compliance. Clients that have urgent needs where time to market is critical, turn to us. Our passion is teaching medical device professionals how to prepare for future regulations and self-monitor compliance, so that they can avoid compliance remediation. https://medicaldeviceacademy.com/ Rob@13485cert.com