Multicompartmental aid devices compliance

In the present study are initially addressed in a general way the regulatory, asistencial and technical aspects related the use of multicompartimental compliance aids. Then, and after pointing out basic topics on stability of re-packaged drugs in those devices, it is widely justified the necessity of having standardized working guidelines in order to avoid any error source. Finally technological aspects regarding the re-packaging are outlined and they are presented, as examples, two standard working guidelines: for thermo-sealing and for permeability determination, as regards USP XXIV rules. Finally, as a conclusion, specific recommendations on pharmaceutical-technological aspects are presented to be counted on for a corrects re-packaging of drugs in compliance aid devices.