Readability User Testing & Co-ordination of Studies
Whereever studies involve test persons or patients the right partner for pharmaceutical industry is Diapharm Clinical Management GmbH. We co-ordinate clinical studies phases I to IV as well as readability user testing of patient information leaflets.
Diapharm sees to it that complex national and international marketing authorization are efficiently implemented. This includes project management tasks for the preclinical studies as well as clinical studies (read more). Medicinal product manufacturers charge us with developing suitable study designs, with co-ordinating suitable Contract Research Organizations (CRO), with statistically evaluating the results and with formulating the final report.
We also provide support to pharmaceutical companies in the sector of readability user testing of patient information leaflets (read more). Comprehensible package leaflets are an important instrument for informing patients and reinforcing confidence. Beate Beime's Diapharm Clinical Management GmbH performs ISO 9001 compliant user testings in the United Kingdom and in Germany. These include
- recruiting the patient target group,
- conducting the single interviews,
- the evaluation, and up to
- filing of the final report ready for submission to authorities.
Prior to testing we also offer text analyses of the package leaflet with the help of a validated program and proposes possible modifications of the patient information leaflet. This way Diapharm prevents comprehension obstacles and minimizes the necessary interview rounds in the customers interest.
