Guideline

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Note for Guidance on Quality of Modified Release Products: A. Oral Dosage Forms; B. and Transdermal Dosage Forms; Section I (Quality)
Internet:	http://www.ema.europa.eu/pdfs/human/qwp/060496en.pdf
Origin/Publisher:	EMEA
Content:	This document concerns quality aspects, especially in vitro testing, of dosage forms in which release of active substance is modified.
Document Type:	CPMP Note for Guidance