Auditing IT Systems for Regulatory Compliance 2018 is a seminar dedicated to regulatory requirements and expectations, and tools for the auditor to ensure the integrity.
Auditing IT Systems for Regulatory Compliance 2018 covers topics such as:
- The details of electronic data and records
- The requirements and expectations by regulators in the medical device, pharmaceutical, and food industries
- Risk-based methodology to the audit process
- Approach to performing a quality audit of a regulated IT system
- Regulated IT system’s validation
- Practical methods for evaluating controls to be placed on suppliers of IT systems and services
- How to write audit findings for regulated IT systems
- How to evaluate a system’s operational usage
Auditing IT Systems for Regulatory Compliance 2018 brings together:
- IT Departments
- Quality Departments
- Quality Auditors
- Validation Teams
- IT Technical staff who specify or develop the systems
- Audit Management
- System owners who are responsible for the systems
- Business process owners whose processes are supported by the systems
