Jeffrey Tate

Dr. Tate has more than 30 years of executive experience in the biopharmaceutical and nutritional supplements industries including drug manufacturing, intellectual property strategy, product development, and cGMP compliance. He retains deep knowledge of food and drug marketing approval procedures, documentation and strategy in U.S. and foreign markets, and implementation of all aspects of regulatory compliance.

He has successfully established integrated regulatory compliance programs resulting in timely, cost effective corporate-wide compliance, meeting regulatory agency requirements and customer expectations in different companies. He closely monitors developments in U.S. and international regulations to maintain compliance and identify regulatory and intellectual property strategies for new products and markets. He holds patents and trademarks in material processing and food formulation.