The U.S. FDAs New Global Engagement Initiative - Webinar By ComplianceOnline (Medical Devices)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Jun 19, 2012 End Date/Time: Jun 19, 2012
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Description

This 90-minute webinar will discuss the new FDA "Global Engagement" Initiative for new areas for heightened CGMP compliance from U. S. FDA-regulated companies and their global partners. It will cover areas for increased awareness, focus, and remediation, and the approaches that are now mandated.

Why Should You Attend:

The last two years have seen major initiatives at the FDA; as well as prominent drug and device failures over cGMP issues, resulting in recalls, lawsuits, class action lawsuits, and even possible criminal prosecution. The FDA sees globalization as a growing reality, and potential contributor of major regulatory issues: the supply chain, counterfeiting, clinical trials, other global outsourcing actions; by global / multinational corporations. A new paradigm for FDA guidance and strengthened enforcement is called for.

This 90-minute presentation will discuss what companies can do proactively to address these concerns and ensure better regulatory compliance from their global partners. You will learn how to translate FDA's current GMPs, as defined in the Code of Federal Regulations ( 21 CFR Part 111, 210/211, and 820), into procedures and work instructions and successfully implement them at off shore partners. We will also discuss failures in globalization and key areas of (cGMP) non-compliance. This webinar will evaluate the new FDA "Global Engagement" Initiative for new areas for heightened CGMP compliance.

Venue

Online Event
2600 E. Bayshore Road
Palo Alto
California
United States
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