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Max Sherman Max Sherman is the President of Sherman Consulting Services, Inc. Before retiring, Mr. Sherman was Vice President, Regulatory Affairs and Clinical Research at DePuy Orthopedics in Warsaw, Indiana. Prior to his position at DePuy, Mr. Sherman was the Director of Regulatory and Clinical Affairs at Zimmer. He is the author and/or co-author of more than 100 professional publications including chapters in books such as The Medical Device Industry, New Drug Approval Process (4th edition), and the Medical Device Packaging Handbook 2nd Edition, a book he edited. His publications have appeared in MDDI, American Pharmacist, Journal of Bone and Joint Surgery, Orthopedic Review, RAPS Focus, U.S. Pharmacist, Food and Drug Law Journal, Pharmacy Times and Clinical Affairs Monitor. Mr. Sherman has taught quality and medical device courses at Butler University, Ivy Tech and Temple University. He recently completed two training modules for ISO 13485, which are now available online. Mr. Sherman has worked in the medical device and pharmaceutical industry for more than 40 years and has been or is a member of the American Society for Quality, the Regulatory Affairs Professional Society, the American Medical Writers Association and the American Pharmacists Association. Mr. Sherman was on the Board of Directors of the Medical Device & Diagnostic Industry Journal and the U.S. Pharmacist. He has been the guest speaker at numerous regulatory conferences and Toastmasters meetings. Mr. Sherman received his Bachelor of Science degree in Pharmacy from the University of Pittsburgh and has taken graduate courses at Purdue University, Wayne State and St. Francis College. |
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