Who Should Attend: GCP and GLP auditors, Quality Assurance, Quality Management, Compliance, and Regulatory Affairs professionals – VPs, Directors, Managers, and/or TrackWise administrators

What You Will Learn:

Traditionally, TrackWise is thought of as a GMP system and is typically deployed within the manufacturing areas of a company. However, TrackWise is designed to be widely applicable and TrackWise solutions can be utilized for the various types of preclinical and clinical quality, compliance, and auditing needs. While you may already use TrackWise for GMP auditing, you can also support GLP and GCP audits within the same electronic system while allowing each to have its own distinct workflow and processes.

The TrackWise preclinical and clinical auditing solutions are designed to facilitate the processes involved with GLP and GCP auditing in addition to providing the standard quality, compliance and workflow management capabilities of TrackWise. Like GMP auditing, GLP and GCP auditing processes can be streamlined and automated with our enhanced auditing capabilities designed to support all audit processes. The structure and flexibility of the various components of the audit process can be tailored to ensure compliance with GLP or GCP regulations. During the hour you will learn:

• The differences between GLP, GCP, and GMP auditing
• How TrackWise can be used for GLP and GCP auditing – best practices for compliance and efficiency
• The benefits of using TrackWise for GLP and GCP auditing
• How GLP and GCP auditing incorporates into your TrackWise EQMS