Pharmacovigilance
This course is designed for undergraduate graduates who aspire to deepen their knowledge and skills in the field of pharmacovigilance and clinical trials. The course provides a detailed understanding of drug safety monitoring processes and methodologies used in clinical research, essential for ensuring the efficacy and safety of drug treatments.
The target group of this course includes professionals from various fields of medical and pharmaceutical sciences, such as pharmacists who wish to expand their knowledge in post-marketing drug monitoring, physicians interested in the clinical aspects of pharmaceutical safety, and licensed pharmacy assistants who want to specialize in pharmacovigilance. The course is also aimed at chemists and chemical engineers involved in drug development and analysis, as well as biologists and biochemists who want to better understand the biological impact of drug substances and contribute to clinical trials.
By participating in this course, professionals will acquire advanced skills in drug risk assessment and management, clinical trial data interpretation, and the application of international regulations in the field. Thus, they will be prepared to contribute significantly to improving the safety and effectiveness of medical treatments.
- Organizers: AVANTYO - Institute of Clinical Research
- Location: Online
- Language: Romanian
- Trainer: Prof. Dr. Viorel Robert Ancuceanu
This course is intended for graduates with a bachelor's degree who wish to deepen their knowledge in the field of pharmacovigilance and clinical trials. It is intended for pharmacists, physicians, licensed pharmacy assistants, chemists and chemical engineers, biologists, and biochemists.
Prof. Dr. Robert Ancuceanu “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
Robert Ancuceanu is a professor within the Bucharest Faculty of Pharmacy (Carol Davila University of Medicine and Pharmacy), where he teaches Cell and Molecular Biology and Pharmaceutical Botany and is currently a vice-dean. With a PhD in pharmacy, a master in biostatistics and a BSc in law, he has worked in different pharmaceutical domains, from academic to industrial and regulatory. He was director general of the General Directorate for Pharmaceutics and Medical Devices within the Romanian Ministry of Health and Vice-president of the Romanian National Medicines Agency. He was a member of the EMA Committee for Human Medicinal Products (CHMP), of the Paediatric Committee (PDCO) and an alternate member of the Committee on Herbal Medicinal Products (HMPC), as well as a member in several committees and working groups in the pharmaceutical field at national level. He is a Steering group member of the TOPRA Product information and Labelling SPIN. He has published over 100 scientific papers (of which 85 indexed ISI Clarivate), two books as a single author and was a co-author or chapter author to 14 books. He is passionate for using computers in the field of life sciences: chemoinformatics, bioinformatics and computational biology, and biostatistics. H-index: 22; citations > 7600. Besides his broad interest for all aspects of the pharmaceutical domain, Robert considers himself a late Renaissance man, having also interests in law, history, music, biostatistics, programming and computer science, sociology, art and literature.
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