We are thrilled to share some exciting news. At MIDI, we have always been dedicated to advancing innovation in the biopharma industry, and during Advanced Therapies Week earlier this month, we were honored by AdvaMed in receiving recognition for our significant contributions.
AdvaMed Acknowledged MIDI as a Biopharma Innovator & Thought Leader:
With the significance of MIDI’s 2023 developments reflected in their latest White Paper, titled “Automated Point-of-Care CAR T-cell Fabrication & Democratization,” by spotlighting MIDI within the dynamic world of biopharma, they have generously shared this latest MIDI White Paper with the AdvaMed and Advanced Therapies community for download.
To access this MIDI WP from AdvaMed, simply click on the link below:
Download the MIDI White Paper:Automated Point-of-Care CAR T-cell Fabrication & Democratization
In 2024 MIDI will continue advancing Point-of-Care CAR T-cell Fabrication by augmenting rapid adoption, early in the R&D cycle, within the biopharma development lab. MIDI has unique modular approaches underway which provide disposable (and paired instrumentation) flexibility within the front-end biopharma development cycle, while providing the benefits of closed-system automated fabrication methodology within the commercialization back-end. This approach will address adoption at all stages of the biopharma development’s life cycle and be unique to this industry. More updates to follow in 2024.
Innovating Healthcare Devices: Navigating Human Factors and User Interface Design
In our next series we will explore the role of human factors and user interface design for medical devices. In this series titled “Innovating Healthcare Devices: Navigating Human Factors and User Interface Design”, Gregory Montalbano, MIDI’s principal, will delve into the crucial aspects of Human Factors and Usability Engineering design in the context of healthcare devices.
The series will provide a comprehensive overview of MIDI’s role as a turnkey medical device development consulting firm. The series begins with an exploration of the who, what, when, where, and whys of Human Factors Engineering, emphasizing its significance in medical device development. We will discuss regulatory considerations and review key elements related to device users, environments, and interfaces. Subsequent podcasts in the series delve into FDA perspectives, regulatory standards, and recommended principles and practices, offering in-depth insights into the intersection of human factors engineering and medical device innovation.
This series will not only provide valuable information for those in the healthcare device industry but also addresses current industry events and trends in human factors engineering.
Stay tuned to the Innovation Vault™ for the first episode coming in February!
We do not share your information with third parties