Success Stories

Navigating Regulatory Complexities: MAE Group’s Strategy for Market Entry with a Mobile Medical App

Goal Project goal was to research and determine regulatory strategy to market a mobile medical app as a diagnostic aid to determine level of cognitive functioning. Background A European startup company developed a mobile device app known as Standardized Mental Capacity Assessment. This app is intended as a diagnostic aid to determine level of cognitive […]

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Regulatory Affairs, Success Stories

Mapping the Path to FDA Clearance: MAE Group’s DHF Compliance Efforts in Renal Dialysis

Goal To determine the gaps in documentation between the existing CE Technical File (and other historical design documents) and the requirements of a design history file (DHF) Background A global premier health care company provides products and services for renal dialysis has designed and manufacturers a therapy system for continuous renal replacement therapy (CRRT), intended

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Regulatory Affairs, Success Stories

From Assessment to Approval: MAE Group’s Journey to CE Marking for Molecular Breast Imaging Devices

Goal The project goal was to secure CE Marking for a Molecular Breast, Imaging medical device according to the European Medical Device Directive. Background A US medical device company developed a molecular breast imaging therapy system used as an adjunct to standard mammography that measure and image the distribution of radionuclides to aid in the

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Regulatory Affairs, Success Stories

Recall Resolution: MAE Group’s Strategic Approach to Knee Brace Safety

Goal The project goal was to lead the global recall of Post-Operative Knee Brace medical device Background A US-based orthopedic rehabilitation products company designs and manufactures, a knee brace intended to control the range of motion at the knee joint following surgeries and other structural repairs. Due to a failure in the mechanical hinge, the

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Regulatory Affairs, Success Stories

Success Story: NeoGuard – Developing a Truly Life-Saving Device

The neoGuard, a first-of-its-kind wearable device vital signs monitor, launched in 2021 in Kenya, Africa. Designed specifically for regions with unreliable electronics and limited resources, neoGuard monitors vital signs in newborns and can alert nurses and doctors of signs of distress, thereby decreasing infant mortality. The neoGuard is the product of a pair of scientist

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News & Blog, Quality System Management, Success Stories
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