Whether you work in pharmaceutical manufacturing, computer science, or the laboratory, if validation and compliance are important to you — don’t miss this event!
IVT's Validation Week is going virtual for 2020 this October! Not to be confused with a single presentation webinar or zoom training, Val Week 2020 brings a completely virtual, 3-day conference experience. With nearly 30 expert speakers and a combination of live and on-demand sessions crafted with your time in mind, the caliber of training content is unrivaled. Here is what you can expect from this year’s Validation Week Event:
REDEFINING YOUR LEARNING EXPERIENCE
In light of the current global climate, it is more important than ever for the quality and validation community to connect with one another, strategize and share ideas – All in a safe, responsible way. With our dedication to address the most pressing issues, the 26th Annual Validation Week has undergone a timely transformation into a fully-digital event taking place October 28 - 30. This virtual event offers attendees the ability to participate in virtual content, exhibits and networking opportunities from the safety of their home or office.
POWERFUL PROGRAMMING ON TAP
Benefit from Two Esteemed FDA Highlights including a session on evaluating emerging trends in enforcement and inspection readiness delivered by Libia Lugo, Drug Specialist, Division of Pharmaceutical Quality Operations Division (FDA) as well as Trends in Oversight and Enforcement: Design Controls and FDARA, delivered by Raymond Brullo, MD, DPM, Compliance Officer, Office of Medical Devices and Radiological Health Operations (FDA.)
Plus, the return of our much loved Empowerment, Diversity and Inclusion Summit featuring thought provoking discussion on “Paving the Way for Progress in Validation,” and of course our Annual IVT Awards Ceremony honoring Validation Trailblazers. Check out the entire agenda.
COMPREHENSIVE CONTENT & CUSTOMIZABLE AGENDA
Benefit from more than 30 thought leaders offering live sessions on important validation topics including process, cleaning and device validation, risk-management, data integrity, and outsourcing. Attendees can customize their own agenda with access to expanded offerings including, on-demand sessions, interactive Q&A sessions, sophisticated and seamless scheduling tools to meet with colleagues, sponsors and regulators, and the opportunity to build your own take-home toolkit choosing from free bonus materials including checklists, templates and white papers. Plus claim up to 15 credit hours toward GMP training requirements. You won't want to miss it!