Harmonisation of regulatory “requirements” for patient preference studies (e22) key regulatory guidance: Under this guideline, most covered federally regulated financial institutions (frfi) are subject to the mandatory exchange of variation margin (vm) and initial margin (im). The revisions consist of two changes (1) a clarification on the treatment of securities issued by entities that receive capital support from the us government, and (2) the extension of the final implementation of the initial margin requirements by one year. Guideline implementation all guidelines quality guidelines safety guidelines multidisciplinary guidelines index of guidelines efficacy guidelines meddra ctd electronic standards (estri) reflection papers & discussion groups consideration documents cioms glossary of ich terms & definitions ich pqkm task force meetings ich calendar assembly. The ich e22 guideline focuses on general considerations for patient preference studies (pps) to inform drug development and regulatory submissions for pharmaceutical products
This guideline aims to optimize the use of pps using a globally harmonized framework.
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