|
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...
|
|