User Consultation – Quotation – Readability Test
Readability report for regulatory submission (1.3.4)
If you need user consultation on your PL, an EMA readability report for your MAA, have any questions or would like to receive a quotation, please do not hesitate to contact Knowhownow. You can contact us here directly, or you can use the RFQ form below for a prompt quotation for your user consultation (AKA Redadability Test) including costs and timing.
Jasper.Moll@Knowhownow.nl or Anna.van.wezel@Knowhownow.nl
Quotation RUT

readability report
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KHN provides EMA compliant reports in English. On request KHN provides your report in French.
User consultation / Readability report Request for Quotation
Services user consultation: Submission-ready 1.3.4 documents (eCTD), Timelines possible between 2 and 10 weeks (respecting your clock-stop slots), Design and printing of mock-up for testing purposes, Testing possible for all European authorities, All PL´s, Rx, OTC and hospital products, CP and MRP, Bridging services, Testing for Patient Instructions, Instructions for Use, Experience with decades of interviewing respondents which results in a pre/test assessment of the readability of the PIL even before the user consultation.