Risk Assessment: Traditional and Novel Approaches to Assess and Manage Risks, Upcoming Webinar Hosted by Xtalks

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In this free webinar, learn the fundamental framework for conducting risk assessments based on traditional and modeling approaches. Attendees will get an overview of the pros and cons of traditional and modern modeling approaches for risk assessment. The featured speakers will discuss case studies intended to illustrate the application of traditional and modeling approaches to risk assessment.

Modeling approaches enable extrapolation of data from preclinical species to humans using established physiological differences.

Risk assessment is a complex process intended to protect human health by identifying drug-related hazards; determining dose-response relations for a product within relevant biological systems; and assessing exposure levels to characterize potential risks. These assessments may be conducted via traditional frameworks using data from in vitro and in vivo studies, as well as novel frameworks using pharmacokinetic and pharmacodynamic model-based prediction.

Risks may be characterized by evaluating the mechanism/mode of action, onset and offset and incidence of clinically relevant hazards. Traditional frameworks put risks into perspective based on the target organs of toxicity identified and the exposure levels at which hazards occurred. The exposure levels at which hazards occurred are used to identify the most sensitive species, which is typically deemed the most relevant species, unless proved otherwise.

Modeling approaches enable extrapolation of data from preclinical species to humans using established physiological differences. These approaches also allow prediction of hazard and exposure in scenarios not explicitly measured in preclinical studies. Modeling frameworks can be incorporated at a very early stage in the development pipeline and can also assist in determining which set of preclinical studies would be most clinically relevant.

Although these frameworks are intended for characterizing and putting potential risks into perspective, each is critical in managing potential clinical risks within relevant contexts to ensure patient safety.

Join the discussion on traditional and novel risk assessment frameworks, the advantages and disadvantages of these frameworks and explore case studies and perspectives on current and future challenges related to them.

Join experts from Allucent, Marcus Delatte, Vice President, Regulatory Strategy, Consulting; Laura Erwin, Regulatory Scientist, Consulting; Manushree Bharadwaj, Senior Pharmacokineticist, Clinical Pharmacology, Modeling & Simulation; and Angela Jeong, Fellow Intern, Clinical Pharmacology, Modeling & Simulation, for the live webinar on Wednesday, November 30, 2022, at 11am EST (4pm GMT/UK).

For more information, or to register for this event, visit Risk Assessment: Traditional and Novel Approaches to Assess and Manage Risks.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

Contact:
Vera Kovacevic
Tel: +1 (416) 977-6555 x371
Email: vkovacevic@xtalks.com

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Vera Kovacevic
Xtalks
+1 (416) 977-6555 x371
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