Customer Success Stories: Literature Reviews and Reg Intel
How CMG MedDev Increased Productivity 3x with MedBoard
Company: CMG MedDev
Industry: MedTech
Location: Spain
MedBoard Solutions Used: Regulatory Intelligence, Literature Reviews, and Clinical Research
CMG MedDev is a tailored MD/IVD consulting service that helps the industry bring products to the market, from the idea to the patients.
With a customer-specific approach, CMG MedDev guides through regulatory affairs services, quality services, clinical research, medical writing services, and many more.
To maintain its competitive edge, CMG MedDev must quickly gather and analyze extensive regulatory and clinical data, a process that traditionally involved labor-intensive, time-consuming manual work. This inefficiency often limited the speed of their deliverables and left team members overwhelmed by routine tasks.
Emilio Llanos González, QA/RA Consultant at CMG MedDev, shared with us their experience in adopting MedBoard for Regulatory Intelligence, Literature Reviews and Clinical Research.
The Challenge
“Before joining MedBoad, finding accurate, up-to-date regulatory information for medical devices and navigating different global requirements was a time-consuming and often overwhelming process. Moreover, I personally struggled with performing literature searches and tracking changes on them, which extended our delivery time and slowed down decision-making.”
Emilio Llanos González, QA/RA Consultant, CMG MedDev
The Solution: MedBoard
MedBoard has fundamentally transformed how CMG MedDev tackles regulatory intelligence and literature reviews, enabling the team to
perform actions 3x faster and increase deliverables within allocated timeframes by 3x or more.
in half the time we did in the past.”
Emilio Llanos González, QA/RA Consultant, CMG MedDev
300+
Systematic Literature Reviews have been performed by CMG MedDev on the MedBoard platform, in only one year.
What do you like best about MedBoard?
“Its speed, its user-friendly interface, its ease of use and
the fact that everything is at the user’s hand,
from simple to more complex tools.
Special mention should be made of its constant updating on regulatory information,
which is published almost in real time on LinkedIn allowing an uninterrupted and updated information flow.”
Emilio Llanos González, QA/RA Consultant, CMG MedDev
Key Benefits for CMG MedDev
Time Savings
CMG MedDev reports that MedBoard
reduces the need
for manual work by
50-75%
making it possible to channel more energy into high-impact, knowledge-based tasks.
Satisfaction
Using MedBoard,
CMG MedDev can focus more on value-added responsibilities. This has translated into
higher
overall job satisfaction, and feeling less overwhelmed.
Collaboration
MedBoard’s automation features and centralized platform foster
improved
communication and internal knowledge leverage. Allowing
CMG MedDev to collaborate seamlessly across projects.
Traceability
The platform’s
strong traceability
features provide
CMG MedDev with
better
evidence management and centralization.
Ensuring that all documentation is secure and organized.
Continuous evolution with MedBoard
“MedBoard’s commitment to continuous improvement is impressive. Since I began using the platform, it has evolved significantly, introducing new features and enhancements that have streamlined my workflow and increased efficiency. At first, literature search interface lacked some features to make easier the task of appraising tons of articles, but in less than 3 months, the MedBoard team solved and make it even easier than before.”
For instance, when I requested a specific feature, the MedBoard team was
highly attentive and implemented the enhancement promptly,
demonstrating their dedication to meeting user needs.”
Emilio Llanos González, QA/RA Consultant, CMG MedDev
A new standard in Regulatory and Clinical Consulting
“MedBoard has been an outstanding change in our way of performing literature searches”
Emilio Llanos González, QA/RA Consultant, CMG MedDev
MedBoard in one or few words?
“A game-changer in regulatory and literature/clinical searches “
Emilio Llanos González, QA/RA Consultant, CMG MedDev
MORE TESTIMONIALS
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