Library of Spanish Presentations on Key Frequently Requested FDA Topics

Library of Spanish Presentations on Key Frequently Requested FDA TopicsCreate a library of presentations in Spanish on key, frequently requested FDA topics (e.g., food labeling, FDA import process, Low Acid Canned Foods (LACF)/Acidified Foods (AF), etc.). The library would include the PowerPoint presentation(s) and/or other appropriate media depending on the subject and the availability of resources. Having important FDA information readily available in Spanish will facilitate compliance with Agency regulations regarding the safety of products exported to the U.S., thereby reducing health risks to the American population.

OIP’s key projects are ongoing but will no longer be tracked in FDA-TRACK. Going forward, on a rotating schedule, the Foreign Offices will summarize their efforts related to outreach, technical assistance, capacity-building, relationship-building, etc. during the Quarterly FDA-TRACK Briefing. The notes from their reports will be documented in the Quarterly Briefing Summary on the FDA-TRACK webpage.

COMPLETED

ON TRACK

A. Select two topics to develop as a pilot project for 2011

3/14/2011

Completed

3/14/2011

B. Collect the basic information and complete the basic PowerPoint presentations

3/14/2011

Completed

3/14/2011

C. Determine the appropriate posting venues and the audience for distribution of materials

3/25/2011

Completed

3/24/2011

D. Define proper exposure format(s) such as webmail, video, CDs and others for each topic)

4/8/2011

Completed

6/1/2011

E. Determine modules and format for the two topics

4/15/2011

Completed

6/1/2011

F. Develop the scripts

4/15/2011

Completed

6/10/2011

G. Complete first draft product for first topic

7/15/2011

Completed

6/10/2011

H. Complete review of the first product (1)

N/A

sub

1. Complete OIP review of first product

8/5/2011

Completed

6/10/2011

sub

2. Complete CFSAN review of first product (1)

N/A

I. Complete first draft product for second topic

9/25/2011

Completed

9/23/2011

sub

1. Complete main modules

8/19/2011

Completed

8/4/2011

sub

2. Complete remainder of first draft product for second topic

9/25/2011

Completed

9/23/2011

J. Complete review of the second product (1)

N/A

sub

1. Complete OIP review of second product

10/15/2011

Completed

10/21/2011

sub

2. Complete ORA review of second product (1)

N/A

K. Post and/or distribute final products based on the venues and audience determined (1)

N/A

(1) Milestones were not completed while this project was tracked in FDA-TRACK.

http://www.fda.gov/AboutFDA/Transparency/track/ucm206185.htmFDA-TRACK Office of International Programs Dashboard