Device Contract Manufacturer and Supplier Management Solutions for Solving Your #1 Headache
Product Details
How would you like to learn about a tool that has been developed to quantify your contractor and supplier risk and make managing them easier?
Plus, this tool would save time and give you a great document to show the FDA to justify your management of your primary and sub–tier suppliers.
Add in straight talk from the FDA regarding trends about contractor and supplier management mistakes for a top-notch, real world solution.
Policing suppliers is a constant headache ... and your greatest challenge. But it doesn’t have to be. We’re here to lend a hand!
A Day of Learning
Clear your calendar for Wednesday, Dec. 14, for a full day of regulatory guidance, plus practical take-home tips and tools to help you work successfully with contract manufacturers and suppliers.
It’s a Virtual Conference, sponsored by FDAnews and featuring top speakers from the FDA and industry. Without ever leaving the comfort of your office, you’ll gain practical knowledge that helps you control the contractors and suppliers you rely on.
You’ll get theory — and practice, too. Every participant will walk away with a workplace-tested quantitative risk assessment tool to apply in their own workplaces for an immediate payoff. Highlights include…
- Melissa Torres of the CDRH’s Office of Compliance kicks off the proceedings with straight talk on the trends the FDA is seeing during inspections and tips on how to avoid running afoul of regulations.
- Consultant Janis Olson of Eduquest, a 22-year FDA veteran and chair of the virtual conference, shows how outsourcing doesn’t mean your validation obligations are over — even if you’ve worked with and trusted a supplier for years.
- Jackie Torfin of Heraeus Medical Components walks you through a case study using a quantitative risk assessment tool to rank a supplier. You’ll be able to create your own copy of the tool to suit your company’s unique demands.
An All-Star Cast
- Melissa Torres, Office of Compliance, CDRH, FDA
- Janis Olson, Vice President of Regulatory and Quality Services, EduQuest (Conference Chair)
- Jacqueline Torfin, Vice President of Quality, Heraeus Medical Components
- Alan Minsk, Leader, Food and Drug Practice Team, Arnall Golden Gregory LLP (invited)
- Deborah Geyman, Senior Manager, Corporate Quality Audit, St. Jude Medical
Here’s How It Works
Twenty-four hours prior to Virtual Conference Wednesday, attendees will receive all presentations.
Then just log on to the Virtual Conference website and dial a toll-free number, both provided in your registration confirmation. And relax. That’s all there is to it.
Washington comes to YOUIn mid December, with the holidays bearing down, boarding a plane for Washington would be a hassle indeed. The Virtual Conference format solves those problems — by bringing Washington to YOU!
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Stress-free! No airport security hassles, no 4 a.m. wakeups, no anonymous hotel rooms. You never even leave your building – not even your own desk.
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Interactive! Constant opportunities to ask questions and get involved. Send in queries via e-mail ... you’ll have answers before you log off.
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Up-to-the-minute! Every speaker operates in the real world, in real time. If news breaks on Virtual Conference morning, you’ll hear about it before the session ends.
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Great value! Spread the word! There’s no limit on number of attendees per site. One low registration fee covers them all. Or register three or more locations for deeper discounts still. Get details here