Webinar: Continuous Organizational Inspection Readiness is a Challenge: How prepared are you?

AN EXCLUSIVE LOOK INSIDE A CENTRALIZED INSPECTION READINESS KNOWLEDGE CENTER

Recorded Monday, September 25, 2017  |  11:00am-12:00pm EDT

If the thought of a regulatory inspection makes you cringe, you’ll want to join this live Webinar. We’ll roll back the curtain on the Avoca Quality Consortium (AQC) Knowledge Center and give you a glimpse of its Inspection Readiness Knowledgebase, a vast repository of leading practices, including agency requirements, guidelines, tools, templates, visualizations, and experience and tips from the 70+ AQC Member companies – all aimed at helping you understand and implement GCP and other GxP standards into your clinical research.

The AQC Knowledge Center is a comprehensive library of over 300 leading practices developed through industry collaboration. Additional features include an online Member community, AQC research reports, and past educational webinars. All contents are geared toward:

• GCP and other GxP compliance
• Operationalizing proactive quality and risk management
• Effective trial oversight
• Technical service provider prequalification standards and tools

• Pharmaceutical companies
• Biotech companies
• CRO companies
• Specialty clinical service providers

Phase of Clinical Research:

• Phase I
• Phase II
• Phase III
• Phase IV

• Clinical Operations/Clinical Development
• Clinical Quality Management/Clinical Quality Assurance
• Vendor Management/Alliance Management
• Clinical Outsourcing/Procurement
• Company Executives
• Clinical trial management
• Clinical Innovation
• Patient Engagement
• Site Level Managers
• Site management (at pharma, biotech, CROs)
• Regulatory Affairs
• Heads of Business Development and Marketing (especially from CROs and vendor companies, for AQC and R&C)
• Inspection Coordination groups

Senior Consultant, The Avoca Group

Executive Director, Avoca Quality Consortium

Senior Consultant, The Avoca Group