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Readability (QRD) Testing of Patinet Information Leaflet (PIL)

Since 2005, marketing authorization holders of medicines are required to have the patient information leafets for their products readability tested. The European Directive 2004/27/EC (a revision of Directive 2001/83/EC) defines

By |2020-04-01T12:49:14+01:00June 4th, 2007|Regulatory Affairs|0 Comments

New Generation of Software for More Efficient Clinical Trials and Multicentre Projects

Beside the software, IT provider will usually provide tailor made adjustment of software and IT support during project. Application will be a user-friendly, scalable and secure. It will run form

By |2020-04-01T12:49:47+01:00August 23rd, 2006|Clinical trials|0 Comments
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