End to End Clinical Operation services
Clinical Operation excellence is the key to each clinical trial success, where NoyMed masters the accuracy and reliability of the provided services coming from 10+ years of experience.
Quality Assurance
Strong Quality Management System/QMS in compliance to regulatory requirements.
Record Management
Fully validated Electronic Trial Master File (eTMF).
Regulatory submissions
Regulatory documentation preparation, maintenance and submissions for all the clinical development stages.
Vendor Management
Vendor Selection, Evaluation, Contracting for study start-up, conduct and close-out phases.
Clinical Project Management
Managing all the study parties communication and successful collaboration during the clinical trial.
Site Selection and Recruitment
Site selection and patient recruitment allowing sponsor to focus on high-quality patient flow for increased efficiency on the trial.
Medical Monitoring
Medical Monitoring ensures the clinical trial patient safety and integrity guaranteed by the quality work of all the clinical trial experts.
Clinical Monitoring
Planning, scheduling, approval and
reporting all investigational site
visits through Visit Planner, overseeing the progress of a clinical trial.