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Clinical Trial Management Service

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Clinical Trial Management Service

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  1. Resolve Medicode Clinical Trial Management Services Creating Future Oriented Solutions

  2. About Us • We partner with you to apply time-tested strategies and next generation solutions. • We help improve health outcomes, drive innovation and enhance efficiencies.

  3. Clinical Trial Management Services • If you are looking for an expert partner to manage your clinical trial, we are at your service. • As a full-service CRO we support you on all levels and in, every step of your clinical research project.

  4. CTMS offers investigators, collaborators and sponsors several benefits, including: Simplify-The powerful site and data management tools, including medidata rave, automate many of the functions for setting up and managing multi-site clinical trials and complex studies.

  5. Streamline-Increased efficiency in data collection, lock down (validation) and analysis shortens the time from study completion to reporting and publication. CTMS tools reduce the administrative burden for investigators and study team members, creating additional capacity for research projects.

  6. Standardize-When completely implemented, CTMS will integrate seamlessly with other Mayo Clinic research and IT systems, and facilitate collaboration with industry sponsors, foundations and federal funding agencies.

  7. Project Management • When we lead your project, our main concern is to release you from any stress related to the project management. • We always keep a strict eye on quality, budget, and timeline. • We are there to make sure, your clinical trial runs smoothly.

  8. What Your Dedicated Project Team Will Do for You? • Plan and execute critical milestones for each study. • Provide excellent customer service and proactive communication. • Identify efficiencies and processes to improve your data quality.

  9. Site Management • We properly review the subject’s safety and the site’s adherence to regulations. • Maintain regular and proactive communication with all parties, at every stage from start-up to close-out. • This collaboration increases the quality of your data and makes sure your trials run efficiently.

  10. Site Selection • The right site meets many needs. • It must fit the sponsors’ needs, but also the study requirements for start-up activities. • Right site is a highly productive site in a suitable geographical location, that can efficiently achieve your goals.

  11. Eligibility • Candidates who have a degree in - life science or bio-sciences, medicine, pharmacy and pharmaceutical sciences, nursing or allied health are eligible.

  12. Reach us https://medi-code.in info@medi-code.in +91 81484 52460 +91 75400 52460

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