Validation Considerations for Mobile Devices in GxP Regulated Life Sciences Applications

During the last 5 years, the rapid evolution of the power and diversity of mobile devices has created new challenges for life sciences company’s IT departments and their regulators. The apparent low cost of adaption and user demand for these devices has upended long held IT and validation standards related to well defined and controlled IT platforms as the basis for the regulatory certainty that underlies IT device qualification regimens.

This white paper will explore the business impacts, regulatory responses and actions to be taken by life sciences firms.

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