Best Practices for Integrity in Clinical Studies
This course covers key principles of medical and scientific writing, including ethical standards, data integrity, and plagiarism prevention.
Participants will learn how to tailor content for various audiences, structure documents (e.g., manuscripts, protocols), and adhere to writing standards such as clarity, consistency, and correct citation. The course also introduces tools for quality control and regulatory compliance.
Benefits of attending
- Understand Good Writing Practice (GWP) standards
- Create clear, accurate, and well-structured scientific documents
- Be compliant with regulatory and industry requirements
Who Should Attend
- Clinical research professionals, including clinical research associates, investigators, and study coordinators
- Medical writers, regulatory writers, and publication professionals
- Quality assurance specialists and compliance officers in pharmaceutical and clinical research organisations
- Anyone involved in clinical trial documentation, regulatory submissions, or scientific publications seeking to improve their understanding of good practices and ethical guidelines
