Information Design & Testing
Through our networks of in-country specialists, we can also provide advice on the regulatory aspects of clinical study design.
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 and have widened our remit to global labelling for pharma / BioTech and MedTech products. For English language testing, we conduct interviews in the United Kingdom, Ireland, and Malta.
We offer the following services:
Study drug 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
For more information please contact us at info@grc-health.com