FDA Pharmaceutical and Medical Device Training and Conferences

Physical Conferences

Conducting Bulletproof CAPA Investigations — ADVANCED
Understanding Advanced Critical Thinking Skills and Innovative Methods to Close CAPA Cases Faster and More Efficiently

Bethesda, MD

Thursday, May 24 - Friday, May 25, 2012

Drug Quality Risk Management
Beyond FMEA — Developing a Comprehensive Risk Toolkit

Bethesda, MD

Tuesday, July 24 - Wednesday, July 25, 2012

Fourth Annual Supplier Quality Management Congress

Bethesda, MD

Tuesday, July 31 - Thursday, Aug. 2, 2012

More Physical Conferences...

Webinars

Pharma Social Media: What You Can and Can’t Do Today
Understanding the FDA’s Recent Guidance and Next Steps

An FDAnews Webinar Rebroadcast

Thursday, May 17, 2012 • 1:30 p.m. - 3:00 p.m. EDT

More Webinars...

Encores

Clinical Trial Training Series

Special 24/7 ENCORE On-Demand Training

Tuesday, Sept. 6 , 2011 - Sunday, Sept. 30, 2012

More Encores...

CDs & Transcripts

Dietary Supplement GMP Inspections and Violations
Tough Talk, Tougher Inspections on the Way

Thursday, April 5, 2012

FDA Import Holds
Black Hole or Bright Spot for Managing Your Imports?

Wednesday, Feb. 29, 2012

Develop a Process Validation Roadmap
Case Studies Show How to Satisfy FDA’s Scrutiny

Tuesday, Feb. 28, 2012

More CDs & Transcripts...

FDA Pharmaceutical and Medical Device Training and Conferences

Physical Conferences

Conducting Bulletproof CAPA Investigations — ADVANCEDUnderstanding Advanced Critical Thinking Skills and Innovative Methods to Close CAPA Cases Faster and More Efficiently

Drug Quality Risk Management Beyond FMEA — Developing a Comprehensive Risk Toolkit

Fourth Annual Supplier Quality Management Congress

Webinars

Pharma Social Media: What You Can and Can’t Do TodayUnderstanding the FDA’s Recent Guidance and Next Steps

Encores

Clinical Trial Training Series

CDs & Transcripts

Dietary Supplement GMP Inspections and Violations Tough Talk, Tougher Inspections on the Way

FDA Import Holds Black Hole or Bright Spot for Managing Your Imports?

Develop a Process Validation Roadmap Case Studies Show How to Satisfy FDA’s Scrutiny

Conferences Search

Conducting Bulletproof CAPA Investigations — ADVANCED
Understanding Advanced Critical Thinking Skills and Innovative Methods to Close CAPA Cases Faster and More Efficiently

Drug Quality Risk Management
Beyond FMEA — Developing a Comprehensive Risk Toolkit

Pharma Social Media: What You Can and Can’t Do Today
Understanding the FDA’s Recent Guidance and Next Steps

Dietary Supplement GMP Inspections and Violations
Tough Talk, Tougher Inspections on the Way

FDA Import Holds
Black Hole or Bright Spot for Managing Your Imports?

Develop a Process Validation Roadmap
Case Studies Show How to Satisfy FDA’s Scrutiny