Lecture:
Application of in vitro in vivo relationships in veterinary medicine: Predicting dose and efficacy, establishing product specifications, and its use in granting biowaivers – examples taken from parenteral extended release products
Tuesday, March 8, 2011 at 14:00 – 15:00 hrs in room U23 building 21, 4th floor
The Faculty of Pharmaceutical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen
Dr. Marilyn N. Martinez, Senior biomedical research Scientist, CVM: Centre of Veterinary Medicine (FDA), USA
Brief summary of Marilyn N Martinez :
Marilyn N. Martinez (MM) received her M.S degree in Zoology/Mammalian Physiology from the University of Maryland (1978). MM earned her PhD from the Department of Physiology and Biophysics, Georgetown University School of Medicine (1983). MM joined the review staff of the Center for Drug Evaluation and Research (CDER), Division of Bioequivalence in 1985. In 1991 MM joined the Center for Veterinary Medicine, and today Dr. Martinez is the Agency´s expert in veterinary pharmacokinetics (PK) and responsible for overseeing the resolution of all PK and biopharmaceutical issues pertaining to the approval and regulation of animal products. She was promoted to the position of Senior Biomedical Research Scientist, a title equivalent to a Full Professor at academic institutions. Dr. Martinez is author/co-author on a significant number of articles and book chapters.
Practical information:
Organized by Claus Selch Larsen, Department of Pharmacy and Analytical Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen, e-mail: csl(at)farma.ku.dk
Participation is free of charge and the lecture is open for attendance by all interested parties. Registration is not required beforehand.
