Teleconference Audio CDs presented by Nancy Singer
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Internal Audits: Meeting FDA Expectations for the Medical Device & Pharmaceutical Industries
-Presented By a Distinguished Panel of Experts, April 14, 2011.
Training Programs: What FDA Expects to See
-Presented By a Distinguished Panel of Experts with FDA & Industry Experience, March 28, 2011.
CAPA: What FDA Needs to See
-Presented by Nancy Singer, Tim Mohn & Betty Collins, December 8, 2010.
Creating Simple, Defensible Documentation to Prove FDA Compliance
-Presented by Nancy Singer and John Avellanet, September 23, 2009.
Making FDA-Required Training Captivating: Training the Trainer
-Presented by Nancy Singer and John Avellanet, August 18, 2009.
Survey Results on Bioresearch Monitoring: Lessons Learned From FDA & Industry
-Presented by a Panel of Experts from FDA & Industry, June 18, 2009.
Do's & Don’ts for Choosing a CRO in Central & Eastern Europe
-Presented by a Panel of Experts from FDA & Industry, September 11, 2008
Do's and Dont's for Choosing a CRO
-Presented by a Panel of Experts from FDA & Industry, June 19, 2008
The Do's & Don'ts of Informed Consent
-Presented by a Panel of Experts from FDA & Industry, Tuesday, April 22, 2008
Implementing an Effective CAPA System: What You Need to Know
-Presented by a panel of experts on March 6, 2008.
Do's and Don'ts: Establishing Supplier Controls & Conducting Supplier Audits
-Presented December 5, 2007 by Nancy Singer and a panel of experts
FDA Panel Meetings: Secrets for Success
-Presented November 1, 2007 by Nancy Singer and a panel of experts
Accessing Internal FDA Information
-Presented August 10, 2006 by Nancy Singer and a panel of experts
Medical Device Advertising: Lessons Learned From Untitled Letters
-Presented February 16, 2006 by a panel of experts.
Medical Devices: Reports of Corrections and Removals
-Presented by a panel of experts on October 26, 2005.
Health Canada Enforcement of Quality System Regulations
-Presented by a Nancy Singer and Egan Cobbold on September 29, 2005.
Getting The Most From Your Internal Audits
-Presented by a panel of experts on July 21, 2005.
Compliance Issues: ISO 13485, QSR & Risk Management
-Presented by Ed Kimmelman, June 16, 2005.
Insights About CDRH’s Office of Compliance
-Presented by Wally Pellerite on May 19, 2005.
A Conversation with Phil Phillips: Insights into CDRH's Office of Device Evaluation
-Presented by Phil Phillips, May 5, 2005.
Device Advertising and Promotion: A Discussion by Industry Experts, April 21, 2005
Challenging the Agency: A Discussion by Former Top FDA Lawyers
-Presented by a panel of experts on March 8, 2005.
2005: States Target Pharmaceutical Promotion
-Presented by a panel of experts on January 27, 2005.
Devices & the Provisions of the Risk Management Standard, ISO 14971
-Presented by Alf Dolan, Stan Mastrangelo and Nancy Singer on December 7, 2004.
510(k)s: Rights and Obligations
-Presented on October 28, 2004 - Various Speakers.