Read the following paragraph extracted from an article from RAPS.org

Read the following paragraph extracted from an article from RAPS.org posted 01 July 2016: http://www.raps.org/Regulatory-Focus/News/2016/07/01/25264/ICH-Adds-14-New-Observers-Adopts-New-Guidelines-at-Lisbon-Meeting/ ”…ICH also endorsed a draft Q&A document aimed at clarifying a 2009 ICH guideline on the non-clinical evaluation of anticancer products (ICH S9 Q&A) that will now be released for stakeholder consultation and are intended to clarify the scope and implementation of the guideline, and support the development and evaluation of medicines for faster access for patients with serious and life-threatening cancers. Two new topics for international harmonisation were endorsed by the ICH Assembly, including the development of a guideline on biopharmaceutical classification system-based biowaivers and bioanalytical method validation, for which recent regulatory requirements have been introduced in the EU, Japan and US…” Which ICH harmonisation activities categories are applicable for each paragraph:

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