FEATURED ARTICLE
Medical Device Regulations – An Update on Things to Come
By Jill E. Sackman, D.V.M., Ph.D.
Over the past several years the medical device industry has been rocked by product recalls, Department of Justice investigations into improper marketing practices, and incidents that highlight the potential conflicts of interest with physicians. As a result, the FDA and Congress are looking at tightening regulations around how products are cleared through the 510(k) process.
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