This refresher course ensures compliance and proficiency in using the platform for study conduct/eReg. Participants will learn to navigate the platform, manage documents, access patient and visit information, manage regulatory documents, sign trainings and documents.
This refresher course ensures compliance and proficiency in using the platform for study conduct. Participants will learn to navigate the platform, manage documents, access patient and visit information, and respond to quality control findings.
This course provides a thorough overview of the informed consent process and Good Documentation Practices (GDP) in clinical research. It emphasizes ethical standards, regulatory compliance (ICH-GCP, FDA), and participant rights. The training includes step-by-step guidance on preparing for and conducting informed consent discussions, handling special populations (e.g., minors, LARs, non-English speakers), and avoiding common errors. It also covers ALCOA+ principles of documentation to ensure accuracy, integrity, and traceability in clinical trial records.
This refresher course ensures compliance and proficiency in using the platform for study conduct. Participants will learn to navigate the platform, manage documents, access patient and visit information, and respond to quality control findings.