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Cato created and maintains the corporate vision. In addition, he directs sponsor interactions, and seeks business opportunities and strategic alliances with other companies and organizations. Cato serves as an advisor on project teams and develops complex strategic development plans and study designs.
He maintains hands-on experience with all phases of the development process, and is especially skillful in devising regulatory and clinical strategies and representing sponsors at regulatory meetings. Cato has more than 35 years of experience in clinical research and new drug development.
Cato has published hundreds of papers, principally in the fields of clinical pharmaceutical research, cystic fibrosis, gene therapy and global drug development.
He serves as a member of the board of directors for several pharmaceutical and biotechnology companies. Sutton has more than 25 years of experience in the drug development industry, specializing in the development of regulatory strategies for drugs and biologics.
She has coordinated activities in various disciplines e. Sutton has been involved in the development of new clinical entities; has overseen the preparation of FDA pre-meeting submissions; and has ensured that regulatory requirements necessary for the approval and launch of new products have been satisfied.
Since cofounding Cato Research inMs. Sutton has served as project leader or project advisor on numerous project teams. In this capacity, she has been responsible for the strategic planning of full development programs for both drugs and biologics in a variety of therapeutic areas.
In her current position, Ms. Sutton provides interpretation, guidance, and advice on regulatory issues; oversees the preparation of regulatory submissions; reviews documents that will be submitted to regulatory agencies; initiates and facilitates FDA interactions on behalf of sponsors; and assists with the development of regulatory strategies.
She has served as the primary regulatory contact for more than sponsors over the last 10 years. As the primary regulatory contact at Cato Research, she develops and coordinates strategies for regulatory agency meetings, and serves as the moderator at these meetings.
Sutton has cofounded several small biotechnology companies and serves as a member of the board of directors for several companies. She has expertise in the development of biological products, with emphasis on gene therapy and blood products, and in the development of oncological, anti-infective, and neuropharmacological products.
Allen Jo Cato, Ph. Cato has more than nineteen years of experience in the development of new drugs in the pharmaceutical industry, with particular expertise in the areas of drug metabolism and pharmacokinetics. Prior to joining Cato Research early inDr. Cato was employed as a clinical pharmacokineticist for more than two years at Ligand Pharmaceuticals, and for four years at Abbott Laboratories.
While in pharmacy school, Dr. Cato spent a year at Burroughs Wellcome where he worked as a member of the data management team on the development of Zidovudine. Cato has been involved in the conduct and analysis of both nonclinical and clinical drug disposition studies, and has been responsible for coordination of the development and validation of several bioanalytical methods.
He has experience with both small molecules and large oligonucleotides, and has contributed to the Human Pharmacokinetics Sections of seven NDAs.
Daniel Cato joined Cato Research in and has extensive experience in project budgeting, project planning, corporate strategy, operations, facilities management, and administration. Chief Financial Officer Mr. Pharand is a Chartered accountant with over 25 years of experience in the pharmaceutical, biotech and life sciences industries where he has a proven track record as a portfolio manager.
He subsequently became an entrepreneur with a successful Canadian distribution company of innovative pedicular screws systems in orthopaedic therapies. Pharand has also acted as a director and has served on various board committees for more than 30 publicly traded or life sciences corporations including Corautus Genetics Inc.
Pharand is also a director of Mistral Pharma Inc. Rotmensch manages the operations of Cato Research Israel and promotes the numerous advantages of conducting clinical trials in Israel and Europe.Grants.
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students, PhD students, and instructors or tenure/track faculty. Organizational Development This Research Paper Organizational Development and other 64,+ term papers, college essay examples and free essays are available now on vetconnexx.com Autor: review • December 24, • Research Paper • 7, Words (30 Pages) • 1, Views4/4(1).
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