Testing for Readability

Considering directive 2001/83/EC, amended by directive 2004/27/EC and legislations which regulate pharmaceuticals marketing rights extension and renewal, we remind you that it is obligatory to do Package Leaflet (PL) readability testing or to produce bridging reports for all pharmaceuticals.

JSC Sveikuva prepares the Package Leaflets and performs PL readability tests according demands of EU legislation and European tests guidelines.

Current methodology of investigation and results systematization of consultations with certain groups of patients allow us to make very clear, comprehensible and easy readable PL for patient and for specialist.

We prepare PL readability tests from 2007. We have already done many orders which were successfully certified by responsible services in Lithuania and other countries.

We are flexible, so we can propose solution which satisfies client’s specific needs at competitive price.

JSC Sveikuva offers readability testing services:

  • Preparation of PL under CMD(h) requirements
  • Analysis of products portfolio and estimate  which products must undergo testing and for which products bridging reports are sufficient
  • Processing of PL readability testing
  • Preparation of bridging reports
  • Writing a final report, in order to have final PL the most exact and understandable
  • PL translations (English, Lithuanian, Estonian, Latvian languages)
  • Professionalism.
    We are specialists in this field and like our activity, so we can guarantee the quality of our work.
  • Competitiveness.
    Individual solutions for a competitive price.
  • Confidentiality.
    We appreciate the cooperation, maintain confidentiality and seek for a long-term partnership