Auditing Analytical Laboratories for FDA Compliance 2017 is a conference that covers topics such as:
- Reviewing Documentation
- GMP Regulations that Apply to Analytical Laboratories
- Auditing Styles and Structures
- Advance Preparation for the Audit
- What to look for while doing a Walk-Through
- Equipment and Laboratory Instrument Qualification
- Following through on the Audit
- Other Regulations and Standards, including ISO 17025
Auditing Analytical Laboratories for FDA Compliance 2017 brings together:
- Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups
- External and Internal Auditors
- Personnel Responsible for Selecting Contract Testing Laboratories
- Supervisors and Analysts in Contract Testing Laboratories
- Consultants