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> FDA Pharmaceutical and Medical Device Training and Conferences
FDA Pharmaceutical and Medical Device Training and Conferences
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FORM 483s
Physical Conferences
FDA Compliance Boot Camp 2012
Validation, Quality and Compliance Training
Clarksburg, MD
Monday, March 26 - Friday, March 30, 2012
Medical Device Risk Management
Beyond FMEA — New Tools To Assure Your Risk Management Program Meets New Standards
Boston, MA
Wednesday, March 28 - Thursday, March 29, 2012
Medical Device Quality & Compliance Institute 2012
Quality Systems and Design Control Training
Clarksburg, MD
Tuesday, April 17 - Friday, April 20, 2012
More Physical Conferences...
Webinars
Pharma/Device Social Media: What You Can and Can’t Do Today
Understanding the FDA’s Recent Guidance and Next Steps
An FDAnews Webinar
Wednesday, Feb. 22, 2012 • 1:30 p.m. - 3:00 p.m. EDT
Requirements for Effective Environmental Monitoring Plans
Six “Must-Have” Factors to Assure Contamination Control
An FDAnews Webinar
Thursday, Feb. 23, 2012 • 1:30 p.m. - 3:00 p.m. EST
Develop a Process Validation Roadmap
Case Studies Show How to Satisfy FDA’s Scrutiny
An FDAnews Webinar
Tuesday, Feb. 28, 2012 • 1:30 p.m. - 3:00 p.m. EST
FDA Import Holds
Black Hole or Bright Spot for Managing Your Imports?
An FDAnews Virtual Conference
Wednesday, Feb. 29, 2012 • 10:00 a.m. - 4:00 p.m. EST
More Webinars...
Encores
Clinical Trial Training Series
Special 24/7 ENCORE On-Demand Training
Tuesday, Sept. 6 , 2011 - Sunday, Sept. 30, 2012
Registering “Applicable Trial” Data on ClinicalTrials.gov
Managing Disclosure of Negative or Non-significant Results
Special 24/7 ENCORE Audio Presentation
Monday, Jan. 30 - Friday, Feb. 17, 2012
Controlling Cross-Contamination in Outsourced Manufacturing
Expert Guidance to Assure CMO Compliance
Special 24/7 ENCORE Audio Presentation
Monday, Jan. 30 - Friday, Feb. 17, 2012
More Encores...
CDs & Transcripts
Managing Data Integrity and Part 11 Compliance for Device Suppliers
Do It Right or Get a Warning Letter
Tuesday, Jan. 31, 2012
Controlling Cross-Contamination in Outsourced Manufacturing
Expert Guidance to Assure CMO Compliance
Thursday, Jan. 26, 2012
Registering “Applicable Trial” Data on ClinicalTrials.gov
Managing Disclosure of Negative or Non-significant Results
Tuesday, Jan. 24, 2012
More CDs & Transcripts...
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