Good Laboratory Practice Compliance Monitoring Summit 2016

Key Topics

• Differences between the FDA and the EPA interpretations and ways of executing of Good Laboratory Practice
• How to prepare your laboratory for an FDA GLP audit
• Maintaining quality standards for employees, infrastructure and testing
• Industry, operational and technical challenges facing Good Laboratory Practice

Who should Attend

Senior attendees from pharmaceutical, medical device and biotechnology companies as well as laboratories with responsibilities in:

• Quality Assurance/Quality Management
• Good Laboratory Practice (GLP)
• Regulatory/Compliance
• Lab Safety
• Laboratory Management
• Audits
• Preclinical Development
• Government Oversight
• Research and Development
• Preclinical Trials
• Product Development
• Global Regulatory Affairs
• Research Labs