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Meetings & Events
| Date |
Location |
Conference |
| January 7, 2009 |
Audio Conference |
The Massachusetts Code of Medical Device Manufacturer Conduct
|
| January 20, 2009 |
Orlando, FL |
Enhancing Safety Risk Management |
| January 20-21, 2009 |
Orlando, FL |
Complaints, MDRs, Reports of Removals & Corrections and Recalls |
| January 21, 2009 |
Orlando, FL |
Risk-Based Strategies for Design Control and Software Validation |
| January 22, 2009 |
Orlando, FL |
Validation of Non-Product Software: Assuring Compliance & Improving Quality |
| January 22, 2009 |
Orlando, FL |
FDA Inspections: What to Expect & What to Do
|
| January 23, 2009 |
Orlando, FL |
Dangerous Documents: Avoiding Land Mines In Your FDA Records and Emails |
| February 17-20, 2009 |
Las Vegas, NV |
Medical Technology Reimbursement Specialist Workshop
|
| February 23-24, 2009 |
Las Vegas, NV |
510(k) Submissions - The Course for Beginning RA Professionals for Preparing a 510(k)
|
| February 25, 2009 |
Las Vegas, NV |
Investigational Device Exemption (IDE) Submission Workshop
|
| February 26-27, 2009 |
Las Vegas, NV |
PMA Submissions Workshop
|
| May 25-27, 2009 |
Rome, Italy |
2009 International Medical Device Industry Compliance, Regulatory & IP Conference |
Inside this section...
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