Dennis M Moore is currently Chief Technical Expert and Managing Partner of Auk Technical Services LTD, Fort Lauderdale, FL. Mr. Moore has 27 years of experience in medical device design, quality systems training, pharmaceutical manufacturing and 21 CFR 210,211 quality systems. Mr. Moore also has extensive experience helping firms achieve compliance to FDA regulation and International Standards regulations. Recent achievements include CE marking a medical device, helping create a Combination Product Quality System; co-authoring a Technical File submission, and achieving ISO 13485:2003 and ISO 9001:2008 certification for a medical device manufacturer. Mr. Moore also functions as a Director of Quality for two medical device client firms.

Mr. Moore has 27 years of experience in medical device design, quality systems training, pharmaceutical manufacturing and 21 CFR 210,211 quality systems. Mr. Moore also has extensive experience helping firms achieve compliance to FDA regulation and International Standards regulations. Mr. Moore has extensive experience as an FDA Investigator, California Medical Device Senior Investigator, Sworn Government-POST Certified Criminal Investigator, Lead Trainer, Compliance Officer and company Chief Technical Expert and CEO.