Interactive adaptive microlearning program developed by a Global Pharma Leader and a Pediatric Center of Excellence (ranked #1 in prescription pharmaceutical and vaccine revenue) to support global education on clinical research requirements, regulations, and best practices.
The Training Division of
Case Study
Global Pharma Leader Pediatric Clinical Research Training Program
PROGRAM AUDIENCE: Clinical research professionals supporting pediatric clinical trials Clinical trial managers, study coordinators, CRAs, investigators, and site personnel Regulatory, medical, scientific, pharmacovigilance, and patient safety professionals
PROGRAM DESCRIPTION:
Interactive adaptive microlearning program developed by a Global Pharma Leader and a Pediatric Center of Excellence (ranked #1 in prescription pharmaceutical and vaccine revenue) to support global education on clinical research requirements, regulations, and best practices. Through six scenario-based eLearning modules, the program helps clinical research professionals strengthen regulatory knowledge, improve decision-making, and apply best practices across pediatric clinical trials.
PROGRAM OBJECTIVES:
Learning Experience Highlights:
h Increase understanding of Good Clinical Practices (GCP) for pediatric populations
h Improve knowledge of pediatric drug formulation, dosing, pharmacokinetics, and patient safety
Six interactive scenario-based eLearning modules
h Strengthen awareness of global regulatory expectations and documentation requirements
Current U.S. and European regulatory guidance
h Support consistent application of pediatric clinical trial processes and best practices
Practical, case-based decision-making exercises
h Enhance learner decision-making through realistic, scenario-based learning
Global education platform supporting consistent clinical research practices
h Promote understanding of innovative pediatric study design approaches across all age groups
Program Components:
Adaptive Microlearning: Developed six interactive, scenario-based eLearning modules designed to improve learner engagement, knowledge retention, and practical application.
Global Regulatory Alignment: Content reflects current U.S. and European pediatric clinical trial legislation, regulations, and industry best practices. Flexible Digital Delivery: Self-paced learning provides a scalable solution for global teams while supporting both foundational and advanced learners.
Realistic Learning Experiences: Immersive clinical scenarios allow learners to apply regulatory guidance and best practices in realistic pediatric research settings.
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info@gomohealth.com
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