Information
Design and Testing
Using our expertise in designing information for patients, we write, design and test patient-oriented materials. This includes documents as diverse as clinical study consent forms, Package Leaflets for marketed drugs and IFUs for medical devices.
During the clinical study phase, we have experience writing, developing, testing, and translating:
Lay summaries of clinical trial results, patient information sheets, dispensing guides, and other supporting written materials for clinical trials.
Patient information sheets and consent forms.
Doctor and patient guides.
Dispensing instructions.
Drug insert information.
Investigator brochure development.
We also have long-standing expertise in the area of Patient Information Leaflet design and readability testing in any EU Member State language. We have widened our remit to global labellingfor pharma / BioTech and MedTech products. For English language testing, we conduct interviews in the United Kingdom and Ireland. We offer the following services:
Label creation and regulatory reviews.
Package Leaflet writing and development.
Readability user testing of Package Leaflets in any EU language.
Package Leaflet bridging statements and reports.
Medication guides and product information testing in the USA and Canada, as well as Australia and New Zealand.
Join us in shaping the future of healthcare
Contact us if you want to find out how we can help you with your project, if you wish to become part of our network of in-country partners or if you wish to take part in one of our studies.
