Ann H. Rose, Dr.PH, is the Founder, Principal & CEO of ViCroTM, a consortium of professionals credentialed in the spectrum of disciplines required for biomedical products (drugs, vaccines, devices, foods, etc) to receive marketing approval and reimbursement. Founded in 1998, the Company assists biopharmaceutical companies, academic institutions and investors evaluate their early development work (pre-clinical, clinical, and manufacturing) conducted on their biomedical inventions. ViCroTM provides the guidance required to attain expeditious regulatory approval to market the product in the U.S and/or other countries. Its core competencies include regulatory, toxicology, clinical pharmacology, medical, clinical trials, statistical analysis, manufacturing, reimbursement, competitive intelligence, intellectual property and licensing. The professionals in these disciplines are pre-imminent in their respective fields and continue daily work at their research bench. In addition, each person has hands on experience with FDA filings.
ViCroTM assures that the Company has a regulatory strategy which is aggressive yet realistic and that it is synergist with the Company's business strategy. Dr. Rose, with more than 25 years in the regulatory environment, is the chief architect of the regulatory strategy. She worked in the Congress of the United States from 1981-1983 assessing health technologies e.g. genetic testing and Phase IV post marketing studies. Thereafter, she joined the Secretary's Office of the Department of Health & Human Services from 1983-1987 as a scientific and health policy advisor. In that position she had oversight responsibilities for FDA, NIH and CDC and served on interagency task forces with the White House Office of Science Technology Policy, Drug Enforcement Agency, Department of State, Department of Agriculture, Environmental Protection Agency, Department of Labor and the National Science Foundation. She was the point person in the licensing of the initial HIV blood test and government-supported AIDS drug development candidates. Through those experiences, she understands the culture, processes and environment of government regulatory agencies. Prior to founding ViCROTM, Dr. Rose held senior corporate regulatory and clinical development positions in the biotech and international biopharmaceutical companies. Dr. Rose earned her Dr. PH. from the University of Texas, her M.S. from Purdue University and her B.A. from Hunter College.
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ViCROTM Headquarters
2600 Pennsylvania Ave NW, Suite 8D
Washington, DC 20037
Phone: (202) 250-6400
Annapolis Office
2195 Chesapeake Harbour Drive East
Annapolis, MD 21403
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