The European Medicines Agency has updated the template for package leaflets to make the information easier for patients to understand. Leaflets will now include less rigid language and new sections that provide greater information about a drug?s benefits. There will also be more information about the medicine?s use in children to comply with the requirements of pediatric regulation.
The European Medicines Agency has updated the template for package leaflets to make the information easier for patients to understand. Leaflets will now include less rigid language and new sections that provide greater information about a drug’s benefits. There will also be more information about the medicine’s use in children to comply with the requirements of pediatric regulation.
The update addresses feedback received during a five-year period of user testing. Stakeholders, including patients, pharmaceutical companies, and national regulatory agencies also contributed their opinions. In addition, the update takes into account the EMA’s 2009 report on the expectations of patients, consumers, and healthcare professionals regarding benefit–risk information, which explains how patients are becoming increasingly involved in choosing their own treatments. In particular, the report called for clear information that is easy to read and understand.
The readability of packaging leaflets and labels is an issue that Pharmaceutical Technology Europe touched upon in May during aninterview with Professor DK Theo Rynor. He explained that a number of commonly-used phrases, such as “Avoid alcoholic drink”, are often misunderstood by patients.
According to a statement from EMA, the update also includes changes to the templates for the summary of product characteristics, labeling and 'Annex II', the section of the product information covering the conditions imposed on marketing authorizations. The updated templates are available in all official EU languages, together with an implementation plan.
VERAXA and Voyager to Create Combined Business for Advancing Pipeline of Next-Gen Cancer Therapies
April 23rd 2025The proposed business combination would create a publicly traded, clinical-stage biopharmaceutical company that will focus on developing a pipeline of next-generation cancer therapies.
Mastering Antibody-Drug Conjugates
December 19th 2024In this episode, we explore BIOVECTRA’s capabilities in antibody-drug conjugate (ADC) manufacturing, from complex conjugation chemistry to synthesis of highly potent payloads. We’ll also showcase how BIOVECTRA’s extensive experience in complex chemistries and specialized small molecule manufacturing gives them a unique perspective, strengthening their approach to ADC production and ensuring clients receive custom solutions across all project stages.
MHRA Approves GSK Therapy Combinations for Multiple Myeloma
April 21st 2025Belantamab mafodotin is approved in combination with bortezomib plus dexamethasone in patients who have had at least one prior therapy, and in combination with pomalidomide plus dexamethasone for those who have had a prior therapy including lenalidomide.
Tokyo University of Science Research Team Explores Improved Delivery of Antisense Oligonucleotides
April 18th 2025Using cholesterol-modified oligonucleotides, the research team aims to improve the delivery of antisense nucleotide-based therapies for treating neurodegenerative diseases and brain cancers.