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This document specifies the framework and the methodology to evaluate and demonstrate the applicability of a validated non-animal method from an OECD test guideline to assess the skin sensitizing potential of a medical device or a medical device material. This document addresses: — the database of reference chemical skin sensitizers and non-skin sensitizers; — reference materials; — feasibility testing of candidate test methods, including any method optimization for use with extracts of medical devices; — prevalidation of candidate test methods; — the interlaboratory study: — sample preparation and coding; — spiking of the extracts from the negative control medical device material; — data collection; — statistical analysis to assess reliability and reproducibility. The use of the approaches described in this document to assess the applicability of a candidate test method does not imply that the candidate test method can be used as a stand-alone test for evaluating the skin sensitization potential of medical devices. For certain candidate test methods, integrated approaches and/or defined approaches are needed.[1] The evaluation of skin sensitization potential of a medical device is described in ISO 10993-10.