We're glad you're here
Welcome
We are delighted to welcome you to our clinical trial team! Your participation as physicians is critical to advancing our research efforts and providing valuable contributions to patient care. Together, we aim to uphold the highest standards of scientific integrity, ethical conduct, and patient safety as we embark on this journey. We are dedicated to supporting you with the necessary resources and guidance to ensure a successful trial experience.
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Why FCN Medical Group?
FCN Medical Group is committed to ethical research, adhering to ICH/GCP guidelines and FDA regulations. We implement rigorous standard operating procedures to ensure responsible and transparent research, consistently meeting or exceeding regulatory standards and maintaining exceptional quality. Our adherence to these procedures builds trust in our research outcomes and reinforces our commitment to excellence.
With over 27 years of experience, we specialize in reducing queries, minimizing errors, and avoiding audit-triggering issues, crucial for achieving high ratings from pharmaceutical clients. Our leadership, having progressed from clinical monitoring to managing clinical programs, focuses on selecting feasible protocols, providing effective staff training, and consistently achieving client milestones. We take pride in delivering clean, reliable data that complies with all protocol and research standards.
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​Our Business Model
Our business model guarantees the highest standards and timely outcomes in clinical trials. Research physicians conduct medical assessments, while FCN Medical Group manages all research activities. This collaboration integrates clinical expertise with research capabilities, enabling us to maintain best practices and achieve positive results.
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How It Works
At FCN Medical Group, our experience and teamwork are crucial to the success of our research projects.
- Mounting queries
- Unprepared monitoring visits
- Missed enrollment milestones
To tackle these challenges, we've streamlined processes that clarify sponsor expectations regarding ICH/GCP guidelines and FDA regulations. Our goal is to simplify operations for the entire research team. We utilize cutting-edge software as our project management tools, ensuring easy access to vital study information, while our project management team helps research staff quickly retrieve details about scheduled patients, study days, and required assessments via our mobile app.
From a business development standpoint, we actively recruit for clinical trials, which increases the number of studies conducted each year. This not only enhances physicians' participation in research but also boosts their practice revenue. Through collaboration with sponsors, we explore new research opportunities that advance medical knowledge and facilitate the development of innovative treatment options.
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What's Next?​​​
Let's connect to answer any questions you have about our business model, research experience, and ethical standards for delivering quality outcomes.
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Thank you for your commitment and collaboration; we look forward to achieving meaningful results together in our clinical trials!
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