John Lehmann, Director of Business Development at IMARC Research
In order to comply with applicable regulations and requirements, the intention of clinical trial monitoring is to protect the rights and well-being of study subjects, ensure data integrity, and ensure that the trial conduct is in compliance with the clinical investigational plan (CIP), agreements, GCP, requirements of the Institutional Review Board (IRB) / Ethics Committee (EC), and all applicable regulations.
In addition, the goals of monitoring should include:
- identifying and addressing non-compliance
- improving quality and promoting high standards
- identifying research misconduct or fraud
What steps can be taken to ensure monitoring goals are achieved? Please take time to download our guide.
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.
The post How to meet clinical trial monitoring goals appeared first on MassDevice.
from MassDevice https://ift.tt/2MvDLlG
Cap comentari:
Publica un comentari a l'entrada