MEDDV 112 - Document Writing for Medical Devices

1. Create coherent text and graphic content for documents used in regulatory-compliant systems. [COMMUNICATE]
2. Explain use of regulatory-compliant electronic or hybrid system requirements for technical writing tasks applied to electronic records and electronic signature document approvals. [COMMUNICATE]
3. Use FDA and other regulatory agency websites as resources for accessing current compliance information. [REASON]
4. Collaboratively develop documents using teamwork skills, writing skills, and regulatory-compliant processes. [EXPLORE]
5. Analyze documentation requirements and respond with the appropriate technical writing solutions and regulatory-compliant processes. [REASON]
6. Present technical information based on best practices oral-presentations. [COMMUNICATE]