Patient Compliance Packaging Q&A
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Asked June 25th, 2009
This question would be best answered by a pharma company. The reason: from a packaging point of view, it would be difficult to speculate on any particular drug’s effectiveness and clinical usage. That said, here is the packaging side’s perspective:
When it comes to compliance packaging playing a role in establishing regimen effectiveness, the pharma companies would determine dosage and if necessary, titration needs. Then it would work with the pharma packager to develop the best means of assisting patient compliance and safety as well as assisting physicians’ control over and monitoring of patient dosing regimen. Assistance can come in the form of a daily annotated peel-and-push foiled package, an F=1 blister package, or any number of other structural design elements. It would again then fall to the drug company to use appropriate protocols and to establish benchmarks and effectiveness metrics to capture, build, and analyze unbiased, comparative data. Innovative packaging can then augment the pharma companies’ ability to be successful as they foster patient compliance.



