In the evolving landscape of clinical trials, ensuring patient safety and data integrity is paramount
Risk-Based Monitoring, or RBM, is revolutionizing how we oversee clinical trials. But what exactly is RBM? IN this video, we’ll uncover the strategies that make RBM a game-changer, reducing risks and enhancing efficiency. Join us as we delve into the principles of RBM and how it’s shaping the future of clinical research. Stay tuned & SUBSCRIBE as we navigate through the intricacies of Risk-Based Monitoring, right here on our channel
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Links to most helpful videos:
CRA Interview: [ Ссылка ]
CRC interview: [ Ссылка ]
Clinical Research Coordinator: [ Ссылка ]
Clinical Research explained under 5 mins: [ Ссылка ]
13 Principle of ICH-GCP: [ Ссылка ]
CRC or CRA: [ Ссылка ]
Phases of Clinical trials: [ Ссылка ]
Good Clinical Practices (ICH-GCP): [ Ссылка ]
Ethics Committee in Clinical Research: [ Ссылка ]
NDCT Rules 2019: [ Ссылка ]
SAE reporting and SUGAM: [ Ссылка ]
Adverse events (AE) in Clinical Trials: [ Ссылка ]
For queries about Advanced Certification in Clinical Research, please reach out/contact at below mentioned platforms
Contact: +91 77219 76079 / 83900 88032
To Register, please click on the link below:
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In this video, We explain about:
(0:00) Intro
(1:18) What is Risk-based Monitoring?
(4:04) Industry guidance for RBM
(6:44) Advantages of RBM
