Assessment templates and guidance - Ancillary medicinal substances incorporated in a medical device
HumanRegulatory and procedural guidanceResearch and developmentMedical devices
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This page lists the Committee for Medicinal Products for Human Use (CHMP) assessment report template and guidance documents used for the assessment of an ancillary medicinal substance incorporated in a medical device.
For queries or comments on templates, please contact: chmp_ar_templates@ema.europa.eu