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Unifying Quality Management. Real-time Management of Adverse Events. Plesha assumed the additional responsibility of leading our Marketing department in December In January , Mr.
Plesha was appointed to the role of President of the Company. Prior to joining the company, Mr. During Mr. Prior to joining Salix, Mr.
Plesha began his pharmaceutical sales career with Solvay Pharmaceuticals where he was a field as well institutional sales representative.
Jeffrey A. Bailey has served as Chair of the Board of Directors of Aileron Therapeutics, a biotechnology company, since March From January to April , Mr.
Bailey has also served as a Director of Madison Vaccines, Inc. From December to March , Mr. From January to June , Mr. Bailey received a B. Mark A. Sirgo Ph.
Sirgo has over 35 years of experience in the pharmaceutical industry, which includes clinical drug development, marketing, sales, and business development, and executive management positions.
Sirgo was responsible for managing the development and FDA approval of Zantac 75 while at Glaxo Wellcome, among other accomplishments.
From to , Dr. Sirgo was added to the Board of Directors of Biomerica, Inc. Prior to joining the company, Ms. Coelho has also served in senior finance leadership roles at Novartis from to She spent the previous twenty years at Mars, Incorporated where she held roles of increasing responsibility and encompassing leadership across all areas of finance and general management.
Lockhart served as Vice President, Pharmaceutical Development and Manufacturing at Salix Pharmaceuticals, where since he established the Pharmaceutical Development and Manufacturing team and contributed to multiple NDA submissions, as well as multiple product acquisitions and launches.
From thru Mr. Lockhart served in various pharmaceutical CMC-related roles and responsibilities at both the Manager and the Director levels of management.
Prior to joining our company, Mr. Before joining Glenmark, Mr. Ostrander held positions of increasing responsibility with Sandoz Inc.
Ostrander has been involved in the issuance of several US patents for his previous contributions in research and development.
James Vollins J. Vollins has twenty-five years of legal experience with over ten years of in-house experience in the pharmaceutical industry, which includes work on several major strategic transactions and a successful initial public offering.
From to , Mr. Vollins was General Counsel, Chief Compliance Officer and Corporate Secretary for Bio Products Laboratory Limited, a UK based manufacturer of plasma-derived therapies, where he helped lead the transformation of the business from a government owned not-for-profit to a high-performing commercial enterprise that successfully launched three new drugs in the U.
Vollins has also worked for other industry-leading pharmaceutical companies, including Grifols Inc. Thomas Tom B. Smith M. His extensive and wide-ranging roles include having served as Chief Medical Officer at various leading pain companies, head of medical affairs at top tier pharma and CRO companies, as well as running his own private practice.
He is a member of several medical societies and organizations including the American Medical Association and the American Academy of Family Physicians.
Smith is a highly published scientific author and has delivered more than presentations in his field of expertise.
Todd C. Davis is Independent Director of the Company.
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