21 CFR Part 11 Electronic Records: Electronic Signatures 2013 is a webinar that covers topics such as:
- Discussion of key requirements
- Detailed review of 21CFR Part 11
- How does an organization assure their systems are compliant
- How should an organization decide which systems fall under this Regulation
- What are FDA Investigators looking for to asses compliance
- What written procedures and training are required
21 CFR Part 11 Electronic Records: Electronic Signatures 2013 brings together:
- Regulatory Managers/Personnel
- Quality Assurance Managers/Personnel
- IT personnel
- Manufacturing managers, supervisors & personnel
- Senior management executives (CEO, COO, CFO, etc.)
- Internal Auditors
- Documentation
- Project Managers
