Learning Management Systems (LMS)

LMS or Learning Management systems have widely been adopted to host training materials and streamline the global training of staff for companies. The need for proper training and documentation of  this training is even more critical for life sciences companies involved in the development and commercialization of products that is governed by global regulatory agencies. Quality Assurance roles require adequate documentation that all staff working in the development of a product whether that is internal staff, consultants, CROs, investigators and study staff involved in clinical trial conduct, etc are trained for the role they serve in the process and have the relevant qualifications to do this. A robust system should allow companies to provide documentation that meets 21 CFR Part 11 requirements and generate reports on compliance meeting the training requirements for each role supporting development. Contact TransPerfect to find out how our LMS can help you assist with meeting your global regulatory training requirements.