Teleconference Audio CDs presented by Michael Palmer

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Clinical Data Aquisition Standards Harmonization Part 2

-Presented by Michael Palmer on January 17, 2008

Clinical Data Aquisition Standards Harmonization Part 1

-Presented by Michael Palmer on January 15, 2008

Leap, Don't Stumble: FDA's New CDISC Reality Explained For Managers & Regulatory Affairs Professionals. Part 2

-Presented by Michael Palmer on June 14, 2007

Leap, Don't Stumble: FDA's New CDISC Reality Explained For Managers & Regulatory Affairs Professionals. Part 1

-Presented by Michael Palmer on June 12, 2007

The CDISC Submission: Ready, Set, Go! Part 2

-Presented by Michael Palmer on March 22, 2007

The CDISC Submission: Ready, Set, Go! Part 1

-Presented by Michael Palmer on March 20, 2007

CDISC Gap Analysis Part 2 - Analysis Data

-Presented by Michael Palmer on January 25, 2007

CDISC Gap Analysis Part 1 - Case Report Tabulation

-Presented by Michael Palmer on January 23, 2007

CDISC Gap Analysis Part 2 - Analysis Data

-Presented by Michael Palmer on July 12, 2006.

CDISC Gap Analysis Part 1 - Case Report Tabulation

-Presented by Michael Palmer on July 11, 2006

FDA's New Demands for Study Data Submissions Part 2. Avoiding the Refuse-To-File Letter: Data Submission Standards and Practices

-Presented by Michael Palmer on March 23, 2006

FDA's New Demands for Study Data Submissions Part 1: Submission Data Requirements and Recommendations

-Presented by Michael Palmer on March 21, 2006

FDA's New Structured Product Label (SPL) Requirement Part 2: Creating the Information Model FDA Requires for All Prescription Drugs

-Presented by Michael Palmer on November 17, 2005.

FDA's New Structured Product Label (SPL) Requirement Part 1: New Requirements for All Prescription Drugs

-Presented by Michael Palmer on November 15, 2005.

FDA Electronic Submissions of Study Data. Part 2: How to be Effective at Building Electronic CDISC Data for the eCTD

-Presented by Michael Palmer on March 2, 2005.

FDA Electronic Submissions of Study Data. Part 1: The "New and Newer" of Requirements and Standards

-Presented by Michael Palmer on March 1, 2005.

FDA Electronic Submissions Part 2: How to Build an eSub

-Presented by Dr. Joshua Sharlin and Michael Palmer on February 3, 2005.

FDA Electronic Submissions Part 1: Essential Requirements and Standards

-Presented by Dr. Joshua Sharlin and Michael Palmer on February 1, 2005.