Mico Holguin graduated from the University of Notre Dame before entering the U.S. Army as an Infantry Officer. After completing several assignments at Fort Bragg, NC, Fort Lewis, WA and Fort Knox, KY, Mico resigned from the Army and held sales positions in Colgate-Palmolive and Abbott Laboratories.
In 1993, Mico transitioned to business development for Abbott Laboratories while representing API and eventually Fill/Finish contract management services. Mico also spent seven years with Cardinal/Catalent in BD also representing Fill/Finish services before recently taking a Pharma Partner Executive position with Baxter Biopharma Solutions.
Mico completed his MBA in 1999 and retired from the U.S. Army after 27 years of Active/Reservist service which includes four years as a member of Special Forces. He resides in Illinois and is a current member of PDA.
Bobby A. Kanuga, Executive Director of External Manufacturing Operations, Merck & Co., Inc.
Bob Kanuga has over 20 years' of experience in manufacturing and business development within the pharmaceutical industry He is currently Executive Director of External Manufacturing at Merck & Co., Inc. responsible for the global supply of outsourced chemical intermediates, active pharmaceutical ingredients, sterile and non-sterile drug products, drug delivery systems and packaging services. Prior to this role, he held many commercial and operations related positions within the company's Manufacturing Division, including Vaccine & Sterile Manufacturing, Global Procurement, and Business Affairs. He received his BS and MBA from Lehigh University.
Richard Korsmeyer, Head of Licensing, Worldwide Pharmaceutical Sciences, Pfizer Global R&D
Richard Korsmeyer has been with Pfizer since 1986 in various roles as a scientist and manager. He is currently a Senior Research Fellow and the Head of Business Development for Pharmaceutical Sciences, where leads a cross-divisional team comprising representatives from Pharmaceutical Sciences (R&D) and Pfizer Global Supply (Commercial Manufacturing), responsible for supporting all Business Development activities including in-licensing, out-licensing, mergers, acquisitions, divestitures, and income-generating initiatives. This team manages all project aspects related to CMC for opportunities from Due Diligence through negotiations and project on-boarding.
As a member of the Technology and Strategic Sourcing organization, he also supports research and technology collaborations and sourcing strategy for R&D stage programs. He maintains a special interest in drug delivery technology.
Richard obtained his Bachelor's degree in Chemistry from Vanderbilt University and subsequently graduated from Purdue University with a Master's and a PhD in Chemical Engineering. Before coming to Pfizer, he worked as a chemist and engineer. He has published in the areas of organic chemistry, polymer science, diffusion, and drug delivery and holds a number of patents. He is a member of American Institute of Chemical Engineers, American Association of Pharmaceutical Scientists, The Controlled Release Society, and the College of Fellows of the American Institute of Medical and Biological Engineering.
For pharmaceutical companies both large and small, the challenges involved in developing new drugs are growing steadily. Regulatory requirements are becoming more complex, and the processes involved have followed suit. Even more innovative manufactur…