How to Conduct a Human Factor Analysis of Instructional Documents, Particularly Master Batch Records (MBR) and Standard Operating Procedures (SOP) 2016 is a webinar that covers topics such as:
- Top Ten FDA Audit Findings
- Human Factors
- Readability/Usability of Instructional Documents, such as standard operating procedures (SOP) and batch records; master batch record/production batch record (MBR/PBR)
- 21 Code of Federal Regulations (CFR) Part 210; 21 Code of Federal Regulations (CFR) Part 211
- Document management system
- Systematic monitoring of effective human factoring analysis of instructional documents by other quality systems
How to Conduct a Human Factor Analysis of Instructional Documents, Particularly Master Batch Records (MBR) and Standard Operating Procedures (SOP) 2016 is intended for:
- Instructional Document Author, Reviewer, Approver
- Leadership Role (regardless of level within organization)
- Continuous Improvement Role
- Document Management Staff
- Manufacturing Operation / Production Staff
- Auditor Role
- Safety Staff
- Training Staff
