Transform drug development through advanced pharmacokinetic modeling and simulation
Advanced Pharmacometric Simulation & Modeling Masterclass is a comprehensive two half-day virtual masterclass designed to foster effective interdisciplinary collaboration between pharmacometricians and scientists involved in non-clinical or clinical drug development.
Whether you're involved in preclinical studies to guide biopharmaceutical development, characterize the pharmacokinetic profile of innovative formulations, optimize in vivo treatment schedules, or conduct clinical research to refine drug delivery, minimize toxicity, and personalize dosing regimens, this course is designed to support your drug development decision-making process.
Through a blend of theoretical frameworks and hands-on workshops, you'll develop practical skills in using specialized pharmacometric software tools, preparing and analyzing PK data, and applying model-based approaches to optimize therapeutic strategies. By bridging the gap between pharmacometricians and researchers, the course promotes effective communication and collaborative decision-making, ultimately leading to more efficient and model-based therapeutic development.
By the end of this intensive masterclass, you will be able to:
WHY JOIN THE EVENT
Bridge theory and application in drug development - Connect fundamental pharmacokinetic principles with practical applications in optimizing therapeutic regimens
Improve interdisciplinary communication - Develop a common language to facilitate collaboration between pharmacometricians and other scientific disciplines
Master specialized pharmacometric software tools - Gain hands-on experience with industry-standard platforms through guided workshops
Enhance data preparation and management skills - Learn efficient techniques for organizing and structuring PK data for robust analysis
Develop model-based decision-making abilities - Apply population pharmacokinetic modeling to inform critical drug development decisions
Design personalized dosing strategies - Explore methods to account for patient variability and optimize individual treatment approaches
WHO SHOULD ATTEND
PK/PD Scientists
Pre-Clinical/Clinical Scientists
Pharmacologists
Regulatory Affairs
ADME/Drug Metabolism
THE CURRICULUM
Engage in meaningful discussions, share insights, and build valuable connections within your industry. Our masterclasses provide a platform to expand your professional network.
Immerse yourself in the latest industry trends and innovations. Our masterclasses feature thought leaders who will share their expertise, providing you with valuable knowledge and perspectives.
Have burning questions or seek clarification? Take advantage of interactive Q&A sessions with our distinguished trainers. Get direct insights and deepen your understanding of key topics.
Attendees gain exclusive access to event-related materials, ensuring you stay informed even after the event concludes. Dive deeper into the subject matter with resources curated for your professional growth.
THE SPEAKERS
Professor Joseph Ciccolini is Full Professor of Pharmacokinetics at the Faculty of Pharmacy, University of Aix-Marseille, Clinical Pharmacologist at the University Hospital of Marseille, and Group Leader of the COMPO Research Team (Inserm Inria) at the Cancer Research Centre of Marseille.
Prof. Ciccolini is currently Chair of the PAMM-EORTC group dedicated to the promotion of pharmacokinetics, pharmacometrics, and pharmacogenetics in oncology. His research focuses on the control of pharmacokinetic variability in oncology and the development of adaptive dosing strategies at the bedside. At the bench, Prof. Ciccolini's work focuses on improving the PK characteristics of anticancer drugs through the development of nanoparticles.
Dr. Anne Rodallec is an Assistant Professor at the Faculty of Pharmacy, Aix-Marseille University, where she teaches the fundamentals of pharmacokinetics and gives workshops on PK modeling to future pharmacists, medical doctors, and health professionals. She obtained her PharmD and PhD in Pharmacokinetics and Oncology at the same university.
She is a tenured researcher at the COMPO research team (Inserm Inria) at the Cancer Research Center of Marseille. Her research background focuses on the development of liposomal drug delivery systems in oncology, encompassing formulation, in vivo evaluation, and pharmacokinetic modeling. Currently, she is investigating the combination of these nanocarriers with immunotherapies to optimize treatment regimens through advanced pharmacokinetic models.
Dr. Rodallec is actively involved in the Controlled Release Society (CRS), where she co-organizes events and facilitates interdisciplinary collaboration among researchers. Her collaborative efforts extend to assisting chemists in developing innovative drugs and determining optimal administration strategies in preclinical settings using model-informed techniques. Recently, she served as a guest researcher at the University of Bonn's Pharmaceutical Development department.
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Yes, participants have access to course materials even after completing the masterclass. We believe in providing ongoing resources to support your continued learning and professional development.
Prerequisites vary by course. While some masterclasses may have specific requirements, many are designed to accommodate professionals at various career stages. Check the course details for specific prerequisites or contact our team for personalized guidance.
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Yes, upon successfully completing a masterclass,you will be awarded a certificate of completion. This certificate serves as a recognitionof your commitment to professional development and mastery in your chosenfield.