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Submitted URL: https://r.wcstrainlifescience.com/mk/cl/f/3lYkBaXPF5Tx_xEWdE5xj0Ewbvfk3FOne-BjvA12SqJfOzyYouIwLCoxa98bEgnq1F0MFyOyiKDaFWItLxXCB5tI...
Effective URL: https://worldcomplianceseminars.com/p/pk-pd-studies-in-drug-discovery-and-development-training?utm_source=sendinblue&utm_campaign=No...
Submission Tags: falconsandbox
Submission: On November 01 via api from US — Scanned from FR
Effective URL: https://worldcomplianceseminars.com/p/pk-pd-studies-in-drug-discovery-and-development-training?utm_source=sendinblue&utm_campaign=No...
Submission Tags: falconsandbox
Submission: On November 01 via api from US — Scanned from FR
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</form>Text Content
Follow us: * Live Webinars * OnDemand * USA Seminars * Europe Seminars * Toll Free 844-267-7299 * More * Seminars * Pharmaceutical Training * About Us * GLP Training * Login * Sign Up PK/PD STUDIES IN DRUG DISCOVERY AND DEVELOPMENT ON 02-NOV, 2022 AT 03:00 PM EDT | 12:00 PM PDT | 02:00 PM CDT DURATION 60 MINUTES Both Live and On Demand Recorded Options Available Purchase Options OVERVIEW PK/PD studies construct, validate, and utilize disease models, drug exposure-response models, and pharmacometric models to facilitate drug development. PK/PD studies offer great support to learn and confirm the key characteristics of new molecular entities in a quantitative manner. This provides evidences for optimizing drug development plans and enabling critical decision-making. Drug development without PK/PD modelling is considered at a higher risk of failure. The webinar reviews the general concepts and basic elements of pharmacokinetics, pharmacodynamics, and their correlation. The use of PK/PD for dose selection during drug development will be described also with the presentation of a case study. The use of PK/PD will be described for the evaluation of both drug efficacy and safety. This will illustrate how the model-based drug development and, in particular, PK/PD studies, can facilitate knowledge management and decision making to streamline drug discovery and development and to reduce the attrition rate. WEBINAR TAKEAWAY * Absorption * Distribution * Metabolism * Excretion * Drug action * Dose-response relationship * Selectivity * Therapeutic window * Biomarkers * Variation in response * Hysteresis * Case study WHO WILL BENEFIT * Project managers * Pre-clinical and clinical pharmacologists * Regulatory affairs * Clinical research associates * Drug discovery scientists FACULTY DR. STEFANO PERSIANI Internal & External Innovation, Director Translational Sciences and Pharmacokinetics at Rottapharm Biotech Italy Dr. Stefano Persiani is currently Director of Translational Sciences and Pharmacokinetics at Rottapharm Biotech, Italy. He graduated in Pharmacy at the University of Milan, Italy and completed a Post-Doctoral fellowship in the Department of Pathology of the University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA, and later as a Research Associate in the Department of Pharmaceutics of the University of Southern California, School of Pharmacy in Los Angeles, California, USA. After these academic positions, he entered the pharmaceutical industry at Farmitalia Carlo Erba, Pharmacia, Upjohn, and Zambon Group and in the CRO sector as Scientific Director for Clinical Pharmacology CHOOSE A PURCHASE OPTION $238.80 EARLY BIRD SINGLE PARTICIPANT LIVE WEBINAR Less You'll have live single user access to log-in of the entire 60-minute webinar, including the Q&A period . You'll also receive all presentation materials. $598.80 LIVE GROUP UP TO 1-5 PARTICIPANTS More You get 1-5 log-in for the live 60-minute webinar for all the participant, presentation materials and the opportunity to ask questions by phone and email $346.80 RECORDED ACCESS SINGLE USER More You'll have 12 month single user access to log-in for an archived recording of the entire 60-minute webinar, including the Q&A period . You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session $478.80 RECORDED ACCESS GROUP More You get 1-5 log-in for the live 60-minute webinar for all the participant, presentation materials and the opportunity to ask questions by phone and email $358.80 LIVE SINGLE + RECORDED More You get one log-in for the live 60-minute webinar for one participant and Access to archived recording of the entire 60-minute webinar, including the Q&A period, for 1 participant. You can log in any time of day or night. Register Now TOP FDA FEATURED COURSES ADVANCED PHARMACOVIGILANCE AUDITING AND INSPECTIONS VIRTUAL LIVE TRAINING COURSE MP3 DOWNLOAD PHARMACOVIGILANCE AUDITING INSPECTION COURSE WILL EXPLAIN HOW TO PREPARE FOR THE AUDIT INSPECTION, OVERVIEW OF THE EUROPEAN MEDICINES AGENCY'S GUID Michael Ramcharan % COMPLETE €3.594 GENOTOXIC IMPURITIES IN DRUG DEVELOPMENT MP3 DOWNLOAD THE WEBINAR PROVIDES A GENERAL OVERVIEW OF THE TOPIC OF GENOTOXIC IMPURITIES AND THE APPROACHES TO SAFETY EVALUATIONS. Dr. Stefano Persiani % COMPLETE $238.80 FUNDAMENTALS OF TOXICOLOGY FOR THE PHARMACEUTICAL INDUSTRY MP3 DOWNLOAD THE WEBINAR WILL COVER THESE ASPECTS THAT ARE RELEVANT FOR NON-TOXICOLOGISTS INVOLVED IN DRUG DEVELOPMENT Dr. Stefano Persiani % COMPLETE $238.80 View All Products * © WCS 2022 * About Us * Contact Us * USA FDA Seminars * Europe Seminars * Pharmaceutical Training * Sitemap * GLP Training * Terms of Use * Privacy Policy Completed Incomplete Incomplete disabled Share Tweet Pin Email Share Share Share Print Powered byPicreel Thank you for subscribing