Ergomed’s Agile and Data-Driven Study Start-Up & Activation Services
Early Planning and Strategic Activation
At Ergomed, early planning is the key to successful study start-ups and site activation. We initiate this planning as early as the Request for Information (RFI) stage. Our approach involves developing a comprehensive study start-up plan refined throughout the bidding process, ensuring it is ready for immediate implementation when needed. This early planning allows us to anticipate challenges and streamline processes, setting the stage for a successful trial.
Global Coverage and Data-Driven Insights
Our global coverage and data-driven approach enable us to quickly identify rapid start-up sites with the best patient populations to achieve the “First Patient In” (FPI) milestone. By leveraging our proprietary intelligence database, we combine historical data, trends, and the latest developments to tailor our study start-up plans. This strategic use of data ensures that we select the most suitable sites and countries for your trial, enhancing recruitment efficiency and success.
Dedicated Study Start-Up Manager
A dedicated study start-up manager with extensive experience in feasibility, site management, and regulatory affairs leads each study start-up project at Ergomed. This manager is your single point of contact, ensuring clear communication and efficient coordination. They take full responsibility for expediting your study start-up and delivering reliable results. With Ergomed, you can rest assured that your study start-up is in the hands of a dedicated and experienced team.
As part of our innovative approach, our study start-up and activation teams:
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Our evaluation analyzes historical data, identifies trends, and incorporates the latest developments to create customized study start-up plans. We can proactively mitigate risks and implement solutions by understanding these interrelated steps and dependencies.
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Our feasibility team, equipped with our intelligence database, identifies the right countries and sites for your clinical trial, optimizing patient recruitment and site performance. This meticulous process ensures we select sites best positioned to deliver high-quality data quickly.
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We identify potential risks early by continuously monitoring and adapting to changing circumstances. We then implement practical solutions to address these risks, minimizing disruptions and ensuring timelines remain on track.
Estimate Your Study Start-Up Timeline With Our Interactive Tool
Do you want to know the possible timelines for your protocol? Use our start-up timelines tool.
Start-up timelines tool
These are estimated timelines based on a number of variable factors. Each project is unique and therefore timelines may be compressed or protracted. We would be happy to provide you with a tailored analysis based on your specific project and target milestones.
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Partner with Ergomed for Reliable Results
Ergomed’s agile, data-driven, and fast study start-up services give you a competitive edge in the clinical trial landscape. Our comprehensive approach, from early planning to proactive risk mitigation, initiates trials quickly and efficiently.
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