People Behind the Platform
Society evolves with technology, and the clinical research industry is no different; it uses technology to develop new tools and treatments to advance medical care. Many clinical research companies have transferred from paper-based trial master files (TMFs) and manual logs to electronic systems and eTMFs. These systems are utilized to assist in keeping documentation compliant and organized. Though these systems make it easier to classify and preserve documentation, they also require a lot of time and effort to ensure proper controls and maintenance. Due to the lack of resources, training and quality control, operating regulatory compliant electronic systems has become an industry-wide issue.
LMK Clinical Research Consulting is a Functional Service Provider specializing in the strategic development, project management and quality control of documents and content that supports clinical development. From study start through completion, our TMF experts deliver quality TMF document management solutions and support to ensure TMF inspection-readiness at all times. Learn more at https://lmkclinicalresearch.com/.