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Home > FDA Pharmaceutical and Medical Device Training and Conferences

FDA Pharmaceutical and Medical Device Training and Conferences

Physical Conferences

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 

FDA Recordkeeping:
How to Prove Compliance and Avoid Dangerous Documents

Boston, MA
Wednesday,  July  17 -  Thursday,  July  18,  2013 

Clinical Trials Disclosure and Transparency Summit
Bethesda, MD
Tuesday,  July  23 -  Wednesday,  July  24,  2013 
More Physical Conferences...

Webinars

Dietary Supplement GMP Inspectional Readiness:
A Comprehensive Road Map To 21 CFR 111
An FDAnews Virtual Conference
Thursday,  June  20,  2013  •  10:00 a.m.  - 3:00 p.m. EDT

Auditing Virtual Suppliers
How to Effectively Avoid an FDA Citation
An FDAnews Webinar
Wednesday,  June  26,  2013  •  1:30 p.m.  - 3:00 p.m. EDT

Device History Records
Sec. 820.184: FDA Inspectors Are Reviewing Them Carefully — Are You?
An FDAnews Webinar
Thursday,  June  27,  2013  •  1:30 p.m.  - 3:00 p.m. EDT
More Webinars...

Encores

Sec. 820.80: Acceptance Activities
The Device Industry’s Silent Problem
Special 24/7 ENCORE Audio Presentation
Monday,  June  3 -  Friday,  June  21,  2013 

Building Quality Into Clinical Trials With Effective Protocol Design
Comprehensive Roadmap To Study Protocol Quality by Design
Special 24/7 ENCORE Audio Presentation
Monday,  June  17 -  Friday,  July  5,  2013 
More Encores...

CDs & Transcripts

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
Tuesday,  April  30,  2013 

GLP and GMP Auditing for High-Potency Compounds
Secrets to Conducting Internal Audits that Assure Compliance
Wednesday,  April  24,  2013 

Newly Proposed EU Medical Device Regs
Understanding the 7 Big Changes That Could Impact Your Device
Tuesday,  April  23,  2013 
More CDs & Transcripts...