FDA Pharmaceutical and Medical Device Training and Conferences

Physical Conferences

Tenth Annual Medical Device Quality Congress
From Risk Management to Postmarket Surveillance

Bethesda, MD

Tuesday, June 4 - Thursday, June 6, 2013

Medical Device Risk Management
Beyond FMEA — New Tools To Assure Your Risk Management Program Meets New Standards

Boston, MA

Thursday, July 11 - Friday, July 12, 2013

From Training to Learning
Improving GMP Performance

Philadelphia, PA

Monday, Aug. 19 - Tuesday, Aug. 20, 2013

More Physical Conferences...

Webinars

Sec. 820.80: Acceptance Activities
The Device Industry’s Silent Problem

An FDAnews Webinar

Wednesday, May 29, 2013 • 1:30 p.m. - 3:00 p.m. EDT

More Webinars...

Encores

Risk-Based Verification and Validation to Meet FDA 820.75 and ISO 13485 Requirements
Best Practices to Move from a Classic Approach to a Risk-Based Approach

Special 24/7 ENCORE Audio Presentation

Monday, May 6 - Friday, May 24, 2013

More Encores...

CDs & Transcripts

Newly Proposed EU Medical Device Regs
Understanding the 7 Big Changes That Could Impact Your Device

Tuesday, April 23, 2013

Complaint Handling Violations for Device Companies
The #1 Warning Letter

Thursday, March 28, 2013

Combination Products cGMP Final Rule
Former FDA Official Helps You Navigate the Combination Products Minefield

Thursday, March 21, 2013

More CDs & Transcripts...

FDA Pharmaceutical and Medical Device Training and Conferences

Physical Conferences

Tenth Annual Medical Device Quality Congress From Risk Management to Postmarket Surveillance

Medical Device Risk Management Beyond FMEA — New Tools To Assure Your Risk Management Program Meets New Standards

From Training to Learning Improving GMP Performance

Webinars

Sec. 820.80: Acceptance Activities The Device Industry’s Silent Problem

Encores

Risk-Based Verification and Validation to Meet FDA 820.75 and ISO 13485 Requirements Best Practices to Move from a Classic Approach to a Risk-Based Approach

CDs & Transcripts

Newly Proposed EU Medical Device Regs Understanding the 7 Big Changes That Could Impact Your Device

Complaint Handling Violations for Device CompaniesThe #1 Warning Letter

Combination Products cGMP Final Rule Former FDA Official Helps You Navigate the Combination Products Minefield

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