Customer Success Stories
New World Medical: Transforming workflows for compliant Literature Reviews
Company: New World Medical
Industry: MedTech
Location: California, USA
MedBoard Solutions Used: Literature Reviews and Clinical Research
New World Medical is a leading innovator in ophthalmic surgical devices, known globally for the Ahmed Glaucoma Valve and Kahook Dual Blade. With a mission to preserve and enhance vision, the company works in close partnership with surgeons and healthcare professionals, developing tools that help improve clinical outcomes and quality of life for patients around the world.
As their product portfolio expanded, the Regulatory team at New World Medical faced increasing complexity in managing systematic literature reviews for their clinical evaluation activities.
Suhail Abdullah, Senior Principal Regulatory Affairs Specialist at New World Medical, with 20+ years of experience inside the company covering R&D and Scientific Management roles, shared with us his experience in the adoption of MedBoard for their Literature Review processes.
The Challenge
“For our clinical evaluation and post market surveillance activities we conduct literature reviews and extract large amounts of data from publications. We were regularly conducting searches on databases, downloading results and extracting data to spreadsheets. This was time consuming and error prone. It was becoming unmanageable as our product portfolio grew.“
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
Transforming workflows with MedBoard
“MedBoard eliminated some of areas where human error was possible.“
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
To address these challenges, the team turned to MedBoard to centralize and streamline their literature review workflows. The platform helped automate repetitive tasks, reduce the risk of human error, and introduce better traceability and collaboration.
“It reduced the number or repetitive tasks we had to do. For example, we saved time in identifying duplicates and creating PRISMA diagrams.“
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
The ability to track tasks and collaborate more easily was especially valuable for a team navigating growing data requirements and evolving regulatory expectations.
“It allowed for better collaboration with team members and tracking of tasks. With everything centralized on MedBoard, our workflow was more efficient.“
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
Why MedBoard?
What stood out most to New World Medical was MedBoard’s thoughtful design and practical functionality to perform compliant literature reviews.
From duplicate detection and customizable screening workflows to automated diagrams and exportable evidence, MedBoard offers everything the team needs to support regulatory compliance without the burden of manual processes.
For New World Medical, having a responsive and knowledgeable support team made a real difference during the onboarding phase.
All you need for Compliant Reviews
“MedBoard has all the features you need to perform compliant systematic literature reviews”
Excellent Customer Support and smooth Onboarding
“The support provided was excellent. The support team helped us overcome any obstacles during onboarding.”
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
What do you like best about MedBoard?
“MedBoard has all the features you need to perform compliant systematic literature reviews. It saves time and helps reduce errors. The support team is great, and they are very receptive to our needs.“
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
MedBoard in one or few words?
“ User friendly. Well designed.”
Suhail Abdullah, Regulatory Affairs Specialist, New World Medical
Ready to Get Started?
Request a free demo today to see how MedBoard can transform your organization and teams