Today's Top SOA Links
From the Wires
FDAnews Announces Device Manufacturing Compliance Crash Course Virtual Conference
By: PR Newswire
Dec. 13, 2012 01:32 AM
FALLS CHURCH, Va., Dec. 12, 2012 /PRNewswire-iReach/ -- Device Manufacturing Compliance Crash Course
FDA inspectors are focusing their attention on very specific violations within device and diagnostics companies. And it's showing up in 483s and warning letters.
Here's a Top 10 list you don't want to be on:
Top 10 FDA Form 483 Citations for Medical Device Firms for Last Year
Tackle these 10 problems and assure smooth sailing through your next inspection.
Join FDAnews Wednesday, Dec. 19, 2012, from 10 a.m. to 4 p.m. EST as we host a virtual conference that will give you concrete knowledge and solutions to the top 10 mistakes device manufacturers are currently making.
If you have questions, we have answers. Register Today
Master device manufacturing compliance in just one day. Here's how.
Featuring six speakers focusing on the trends, FDA regulations and best practices for avoiding mistakes, attendees will come away with ideas on how to transform their device manufacturing compliance problems.
Get answers to your toughest questions — in just a day. No travel required. Gather your colleagues for the best, and most cost effective, training in the industry.
Your virtual conference chairperson is James Wason, Ph.D, principal of Maelor Group Lifesciences Consulting. Dr. Wason has more than 35 years of experience working with device manufacturers.
10:15 a.m. – 11:00 a.m.
11:00 a.m. – 11:45 a.m.
11:45 a.m. – 12:00 p.m.
12:00 p.m. – 12:45 p.m.
12:45 p.m. – 1:30 p.m.
1:30 p.m. – 2:30 p.m.
2:30 p.m. – 3:15 p.m.
3:15 p.m. – 4:00 p.m.
The virtual conference is convenient to attend. All that's required is that you be in front of a computer monitor at the appointed time, whether you're at the office or telecommuting from your office-in-home.
Of course, the panel of experts will be on hand to answer all of your questions. Simply submit your questions via email, and you'll have answers by the time the session ends.
Everyone in your organization with a role in product development, legal and regulatory affairs will benefit from taking part in this event — and they can do so at a cost that won't break the budget. You pay a single low registration fee per facility, regardless of how many participate. So spread the word.
Sign up for Medical Device Compliance Crash Course today.
Who Will Benefit
Meet Your Instructors
Here's How It Works
Key people throughout your company will benefit from taking part in this event. Best of all, everyone can do so at a cost that won't break the budget. You pay one low registration fee per facility, regardless of how many participate. So spread the word.
Don't take unnecessary risks. Sign up today for this timely learning event.
4 Easy Ways to Register
By phone: 888-838-5578 or 703-538-7600
Mail to: FDAnews
Web 2.0 Latest News
|| | | | | | ||
| | | |
| | | |
| | | |
| | | |
| | | | | | | | | |
|SYS-CON MEDIA: | | | ||
|SYS-CON EVENTS: | | | | ||
|INTERNATIONAL SITES: | | | | | | | | | ||
|Copyright ©1994-2008 SYS-CON Publications, Inc. All Rights Reserved. All marks are trademarks of SYS-CON Media.|
|Reproduction in whole or in part in any form or medium without express written permission of SYS-CON Publications, Inc. is prohibited.|