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Presenter: Dr. Bernard A. Olsen, Olsen Pharmaceutical Consulting, LLC Organic impurity levels can be measured by a variety of techniques, including those that compare an analytical response for an impurity to that of an appropriate reference standard or to the response of the new drug substance itself. In cases where the response factors of the drug substance and the relevant impurity are not close, this practice can still be appropriate, provided a correction factor is applied or the impurities are, in fact, being overestimated. In this webinar we look at the rationale for using RRFs and potential errors in RRF determination, including robustness and salt form issues, as well as the impact an incorrect RRF can have. Download the slides for the webinar here: https://www.lgcstandards.com/GB/en/Re... ********* Follow our channel and join the discussion with us on social media to stay up to date with our latest news, highlights and industry insights: LinkedIn - https://www.linkedin.com/company/lgc-... Twitter - https://twitter.com/LGCStandards?utm_...