Securing new drug development by establishing and maintaining phase-appropriate RSM designation from development to commercial launch

Securing new drug development
This webinar will discuss WuXi STA’s practice on overall RSM strategy, focusing on: Starting material evolution, RSM designation, Risk mitigation for potential regulatory push-back
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OTHER ON-DEMAND WEBINARS

Utilizing NGS for Proteomics - Olink® to Accelerate Drug Discovery and Optimize Clinical Trials Outcome

The future of healthcare will change for the better by adding more tailored treatment options, where patients get the best medication related to their disease state and predisposition.
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Overcoming Challenges in Ophthalmic Drug Delivery Including Bioavailability and Sterility

Pharmtech

Delivery of therapeutics to the human eye is one of the most interesting—but challenging—endeavors a formulator can take on. The anatomy and chemical composition of the eye make it highly resistant to pharmaceutical penetration. Successfully circumventing these protective barriers requires intimate knowledge of ocular delivery as well as specialized development and manufacturing expertise.
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Integrating Polygenic and Monogenic Germline Testing Results Into Prostate Cancer Risk Assessment

Ambry Genetics

In this webinar, Dr. Xu will summarize recent data on inherited risk for prostate cancer, including germline mutations in high-penetrance genes (HPGs), risk-associated SNPs, and SNP-based genetic risk score (GRS). He will present detailed data supporting the broad-sense validity of GRS in risk assessment as well as the need for assessing the narrow-sense validity of GRS values. Finally, he will review the data supporting the importance of GRS when estimating the penetrance of HPGs.
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Study Designs and Statistical Methods for Assessing the Genetic Architecture of Disease

Ambry Genetics

An introduction to study designs for investigating the role of genes in disease will be provided, followed by an overview of statistical methods used to test hypotheses for each design. Examples of several designs will be discussed, as well as accompanying methods. Publications assessing the role of genetic variation in disease will be examined, and a critical critique of methods and results for each publication will be reviewed.
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