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.