Improving patient adherence is a constant concern for every device manufacturer. Our expert, Andreas Meliniotis, Director of Device Development, writes about how ‘human factors should be implemented to ensure that any possible design issues are rectified before production’.
In his recent article published by Pharmaceutical Manufacturing and Packing Sourcer, November 2020 edition, titled “Battling ‘Operating Error'”, Andreas highlights the importance of human factors studies during the device development process, as they provide valuable insight on how devices will be handled by the target population.
You can download the full article here.
This article is taken from Pharmaceutical Manufacturing and Packing Sourcer November 2020, pages 30-33. © Samedan Ltd