2013 FDA Training Schedule and Registration


SPL Training Sessions (live web and audio)
Registration Information
Note: Requests for registration for the 2013 SPL training sessions should NOT be submitted PRIOR to Monday, January 21, 2013.
There is no registration fee for the training sessions but pre-registration is required because of limited connections for the webinars. To register, please submit the following information via e-mail to spl@fda.hhs.gov:
  1. Attendee’s first and last name
  2. Name of your organization
  3. Session name and date of training session(s) for which you are registering.
You will be limited to one phone/web conference line per company.
For further information, contact: spl@fda.hhs.gov.

2013 SPL Training Sessions
The 2012 SPL training sessions are scheduled Mondays from 11:30 a.m. - 12:30 p.m., ET on the following dates:

  • Session 101 - February 11, 2013 – New SPL Xforms
  • Session 102 - February 23, 2013 – NDC Labeler Code/Establishment Registration SPL
  • Session 103 - March 11, 2013 – Content of Labeling/Product Data Elements SPL Part One: Content of Labeling Sections – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)
  • Session 104 - March 25, 2013 – Content of Labeling/Product Data Elements SPL Part Two: Product Data Elements – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)
  • Session 105 - April 8, 2013 – Bulk Ingredient/Bulk Product SPL
  • Session 106 - April 22, 2013 - SPL for Advanced Users
  • Session 107 - May 6, 2013 - New SPL Xforms Session 108 - May 20, 2013 - NDC Labeler Code/Establishment Registration SPL
  • Session 109 - June 3, 2013 - Content of Labeling/Product Data Elements SPL Part One: Content of Labeling Sections – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)
  • Session 110 - June 17, 2013 - Content of Labeling/Product Data Elements SPL Part Two: Product Data Elements – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)Bulk Ingredient/Bulk Product
  • SPLSession 111 - September 9, 2013 - New SPL Xforms
  • Session 112 - September 23, 2013 - NDC Labeler Code/Establishment Registration SPL
  • Session 113 - October 7, 2013 - Content of Labeling/Product Data Elements SPL Part One: Content of Labeling Sections – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)
  • Session 114 - October 23, 2013 - Content of Labeling/Product Data Elements SPL Part Two: Product Data Elements – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)
  • Session 115 - November 4, 2013 - New SPL Xforms
  • Session 116 - November 18, 2013 - NDC Labeler Code/Establishment Registration SPL
  • Session 117 - December 2, 2013 - Content of Labeling/Product Data Elements SPL Part One: Content of Labeling Sections – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)
  • Session 111 - December 16, 2013 - Content of Labeling/Product Data Elements SPL Part Two: Product Data Elements – Human and Animal Rx & OTC Drugs (including homeopathic, medical gas, and repacked and relabeled drug products)