Monitoring Services
Independent Clinical Research Monitoring
Why our monitors:
The collaboration between you and our clinical research monitor is aligned with the specific requirements of your project. Our monitors remain consistently accessible throughout the entire project duration, prioritizing your project needs above all else.
On-Site Monitoring Visits
Remote Monitoring Visits
Monitors are ready to carry out site qualification visits, site initiation visits, interim monitoring visits, and close-out visits in accordance with the approved protocol.
Monitors are prepared to prepare and submit the necessary documentation (confirmation letters, follow-up letters, trip reports) as outlined in the clinical monitoring plan (CMP).
Monitors comply with the guidelines and regulations set forth by Institutional Review Boards and Regulatory Authorities.
Case Report Form (CRF) Review
Encompasses the review and verification of source documentation, generation and resolution of queries, and ensuring accuracy in safety reporting.
Phase I - III Clinical Research Experience
Various therapeutic areas of expertise are available.
Vaccines
Infectious Disease
Respiratory
Normal Healthy Subjects
Neurodegenerative Diseases (CNS)
Women's Health
Oncology
Travel, including air travel may be arranged.
Ready for both domestic and international travel, we stand prepared to meet the requirements of your global project.
©NaLiRo Clinical Research, LLC
Hours of Operation:
9:00 am–5:00 pm, Monday - Friday
Phone: 443-769-7274
Email: nross@naliroclinicalresearch.com