Clinical Monitoring
At CAN-AM Research, LLC we have established a network of experienced CRAs to meet the varied monitoring needs of our clients. Each of our team members has over 10-years of experience monitoring clinical trials at all phases, covering a wide range of therapeutic areas. This team of experienced, committed and dedicated CRA's will see the projects through to completion, focusing on the needs of our clients and delivering with the highest of standards. Whether you require 1 or 20 CRA’s, we are a collaborative network that can meet your needs and deliver exceptional quality in our work.
Monitoring Capabilities
Our clinical monitoring services include but are not limited to:
Monitoring Capabilities
Our clinical monitoring services include but are not limited to:
Project Management
Our team of project managers will guide your project by preparing protocols, case report forms, other study documentation, IRB/ethics review committee approval, development of recruitment strategies to increase patient enrollment into the trial, the provision of clinical trial materials, and the overall management of the trial. Our team ensures full compliance with all aspects of ICH/GCP - from project award to project completion.
Auditing of Clinical Trials
Per the ICH guidelines, our auditors will conduct a “systematic and independent examination of project related activities and documents to determine whether the evaluated trial related activities were conducted and the data were recorded, analyzed and accurately reported according to the protocol sponsor, SOPs, GCP and applicable regulatory requirements."
Please contact us to learn more about how we can serve your clinical development needs.