Biometrics
End-to-end Clinical Operations Solutions
NoyMed’s Clinical Operations capabilities are covered through a network of trusted and qualified partners allowing global coverage.
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.
See other solutions
Biostatistics - PK/PD Analysis
NoyMed’s team of expert Biostatisticians have years of experience in supporting trials with ...
Full Data Management
NoyMed's experienced team of Data Managers covers everything from the DataBase Build through Conduct ...
Medical Writing
NoyMed's Medical Writing services include all the key aspects of studies - from Protocol Development to CSRs ...
SAS programming & CDISC Conversion
Our Flexible and Efficient SAS Programming team is experienced in preparing CDISC packages across ...
End to End Clinical Operations
NoyMed's Clinical Operations capabilities are covered through a network of Trusted and Qualified ...
Pharmacovigilance
NoyMed’s professional team of Pharmacovigilance specialists has 10+ years of expertise and valuable ...
