Multidisciplinary: nanomedicines

The European Medicines Agency's scientific guidelines on nanomedicines help medicine developers prepare marketing authorisation applications for human medicines.

For a complete list of scientific guidelines currently open for consultation, see Public consultations.

Guidelines

• Data requirements for intravenous iron-based nano-colloidal products developed with reference to an innovator medicinal product
• Data requirements for intravenous liposomal products developed with reference to an innovator liposomal product
• Development of block-copolymer-micelle medicinal products
• Surface coatings: general issues for consideration regarding parenteral administration of coated nanomedicine products