Consumables
Intergraf calls for the retention of paper leaflets in medicinal products
Monday 06. November 2023 - Intergraf takes a stand in defence of consumer rights, particularly those related to medicinal products for human use. Intergraf urges the EU to reconsider Article 63.3 of the proposed Directive on Medicinal Products, emphasizing the role of medical leaflets in pharmaceutical packaging.
Accessibility and patients’ safety
The legislative proposal under consideration aims to ensure the accessibility and safety of patient information in a digital format. While this goal is commendable, Eurostat 2023 data point out the stark reality that 70.7% of Europeans possess only basic, low, or no digital skills, whereas 7.5% of European households have no internet access. Thus, the reliance on digital access to medication information risks excluding many patients, particularly those who are vulnerable due to age, lack of digital skills, or limited resources. The advancement of the digital healthcare system should not result in the exclusion of a significant part of the population; it is crucial to prioritize the safety and health of all patients.
Patient’s right to printed leaflet
Article 63.3 proposes that patients can request free printed copies of digital-only package leaflets. However, this idea lacks practical implementation solutions. Pharmacies cannot meet the rigorous printing standards and security requirements for medical leaflets, unlike industrial-level processes in the pharmaceutical industry.
Printed and digital leaflets are not mutually exclusive
Intergraf underscores the importance of complementarity between electronic product information (ePI) and paper leaflets. ePI enhances access to medicinal information for some demographics but cannot replace paper leaflets accompanying medicines. The exclusive use of ePI should only be considered in exceptional circumstances, such as when medicines are administered by medical professionals, like in-hospital patients.
In light of these concerns, Intergraf calls for the mandatory retention of paper leaflets in the packaging of medicinal products.