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