Quality requirements for drug-device combinations | European Medicines Agency
* DDCs within the scope of this guideline are medical devices that are integral to the medicinal product, co-packaged with the medicinal product or referenced in the medicinal product information and obtained separately.
https://www.ema.europa.eu/en/docume...-requirements-drug-device-combinations_en.pdf
* DDCs within the scope of this guideline are medical devices that are integral to the medicinal product, co-packaged with the medicinal product or referenced in the medicinal product information and obtained separately.
https://www.ema.europa.eu/en/docume...-requirements-drug-device-combinations_en.pdf