David Shields has spent his career gaining experience in the pharmaceutical industry. He has extensive expertise in analysis of medical device/drug product interactions and experience in GMP/GLP contract manufacturing, analysis of pharmaceutical active ingredients (small & large molecule), and pharmaceutical formulations (tablet, gels, parenterals, transdermals). As well as experience in developing successful business interactions and intellectual property strategies. He is also familiar with clinical development and regulatory issues as they pertaining to preparation of documents and facilities for IND, NDA, BLA and foreign filings.
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