The road to bringing a medical device to market is fraught with potential regulatory pitfalls and decisions that can delay—or even derail—your efforts.
The road to bringing a medical device to market is fraught with potential regulatory pitfalls and decisions that can delay—or even derail—your efforts.
StageBio clients often ask for expert guidance when it comes to developing a protocol for the pathology work of their medical device studies. Senior Pathologist Lynette Phillips, DVM, PhD, DACVP, held a live webinar event to demystify several preclinical pathology operations which are crucial to a study’s success.
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