How to Prepare for and Manage Audits/Inspections across Global Markets

This on-demand webinar, hosted by Greenlight Guru, features a panel of medical device industry experts engaging in a lively discussion about audits and inspections. Learn essential strategies to ensure your organization is audit-ready and compliant with international regulations.

Main points covered:
1. Understanding global regulatory requirements and standards for medical devices
2. Key steps to prepare for audits and inspections
3. Effective documentation and record-keeping practices
4. Strategies for managing on-site audits and inspections
5. Post-audit follow-up and continuous improvement

Target Audience:
• Quality Assurance Managers
• Regulatory Affairs Specialists
• Compliance Officers
• Medical Device Manufacturers

Access the printable slides for this presentation by visiting: www.greenlight.guru/webinar/how-to-prepare-for-and…