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Planning Made All The Difference: FDA Web Taxonomy Case Study

This case study explores how the U.S. Food and Drug Administration (FDA) revamped its website to be person-centric, informative, empowering, and interactive. The project aimed to define a cross-functional taxonomy, categorize information efficiently, and improve content management. From project kick-off meetings to taxonomy testing and training, the FDA worked diligently to create a user-friendly web experience. Through taxonomy validation exercises, the FDA confirmed staff could effectively tag content, improving searchability and organization on the site. The study highlights the benefits of the taxonomy project in breaking down organizational barriers, facilitating teamwork, and enhancing content discoverability.

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Planning Made All The Difference: FDA Web Taxonomy Case Study

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  1. Planning Made All The Difference: FDA Web Taxonomy Case Study U.S. Food and Drug Administration Working together to create a Web site that is… • Person-centric • Informative • Empowering • Interactive September 25, 2008 FDA Internet Improvement Team (FIT)

  2. Overall FDA Web Taxonomy project goals • To define a programmatic cross-functional taxonomy (classification scheme & controlled vocabularies) that supports FDA’s metadata specification and applies to FDA content overall. • Provide a single methodology for categorizing information across FDA offices, programs and regions. • Reduce the time it takes to successfully target and find cross-Office information. • Improve FDA’s ability to find, use, manage and publish FDA content on the Web • To train, guide and support FDA in testing and implementing the taxonomy.

  3. FDA Web Taxonomy project Kick-off meetings (8/3) 1 Discovery Resource Review 2 Metadata Specification Revise Spec Third taxo workshop (12/11) 3 Vocabulary Development Build-out Revise Taxo Review Taxo Strawman Build-out Extreme Review Review Taxo Finalize Taxo Review Taxo Build-out 4 Testing Extreme taxo workshop (8/14-17) First taxo workshop (10/18) Second taxo workshop (10/18) 5 Training & Guidance Factsheet Draft Process & Guidelines 8/6 8/13 8/20 8/27 9/3 10/19 10/26 11/2 11/9 11/16 11/23 11/30 12/7 Inside.FDA project FDA.gov project

  4. FDA Web Taxonomy project (2) 1 Discovery 2 Metadata Specification Taxonomy testing (12/15-16) Finalize Taxo 3 Vocabulary Development 4 Testing Devise Test Test Review Test Analyze Test 5 Training & Guidance Taxonomy Governance Training Mats 12/14 12/21 12/28 1/4 1/11 1/18 1/23 1/30

  5. FDA Taxonomy facets

  6. FDA Taxonomy facets & sub-facets FDA Taxonomy Content Types Subjects Audience Geographic Activities FDA Org Laws Diseases Products Brands Companies Topics

  7. Taxonomy-driven portlets LANGUAGES = “es” REGULATED PRODUCTS = “Food” INDEXES = “A-Z Indexes” REGULATED PRODUCTS = “Drugs” REGULATED PRODUCTS = “Medical Devices” REGULATED PRODUCTS = “Animal & Veterinary” REGULATED PRODUCTS = “Biologics” REGULATED PRODUCTS = “Cosmetics” REGULATED PRODUCTS = “Combination Products” AUDIENCES = “All” FDA ORGANIZATION = “All” CONTENT TYPE = “Job Information” FDA ORGANIZATION = “Advisory Committees” CONTENT TYPE = “Transcripts & Statements” CONTENT TYPE = “Budget” DATE = “Latest” CONTENT TYPE = “News”

  8. Taxonomy-driven portlets CONTENT TYPE = “Product Approvals” DATE = “Today” to “Today-30” ORDER BY DATE CONTENT TYPE = “Recalls” REGULATED PRODUCTS = “Pet Food” ACTIVITY = “Consumer Health” SUBJECT = “Drug safety” CONTENT TYPE = “Recalls” OR “News Releases” ODER BY = “Date” CONTENT TYPE = “Research Reports” ACTIVITY = “Clinical Trials” CONTENT TYPE = “Dockets” OR LAWS = “All” ACTIVITY = “Toxicological Research” CONTENT TYPE = “Comments” CONTENT TYPE = “Product Approvals” CONTENT TYPE = “Guidance Documents”

  9. Taxonomy-driven portlets CONTENT TYPE = “Recalls” ODER BY = “Date” LANGUAGES = “es” INDEXES = “A-Z Indexes” TAXONOMY TERM = “Regulated Products” ORDER BY = “BT” CONTENT TYPE = “Handling Complaints” CONTENT TYPE = “Product Approvals” FDA ORGANIZATION = “All” AUDIENCES = “All” CONTENT TYPE = “Budget” DATE = “Latest” ACTIVITY = “Clinical Trials” FDA ORGANIZATION = “Advisory Committees” CONTENT TYPE = “Job Information” CONTENT TYPE = “Dockets” OR LAWS = “All”

  10. FDA.GOV Taxonomy example: Information about what to do about bad spinach.

  11. FDA.GOV Taxonomy example: Information on Accutane for a patient.

  12. FDA Taxonomy validation exercise • Demonstrate that FDA staff will be able to use taxonomy to easily tag content. • Validation tests: • Place 40 popular terms from Google query logs in the correct Taxonomy facet. • Tag content from a test collection and compare those tags to an established baseline. • 14 items selected from over 100. • Half intranet, half internet. • 16 FDA content managers participated.

  13. Blind sorting of popular search terms Results: Very Good 72% of terms were correctly sorted 75-100% of the time. • Difficulties • Brand vs. Company names, e.g., Colgate. • Brand names vs. Product categories, e.g., Aspartame. • Content types (there are definitions & synonyms in taxonomy) • Facet definitions

  14. Content tagging consensus Results: Very Good Test subjects tagged content consistent with the baseline 73% of the time. • Observations • Many other tags were reasonable alternatives. • Correct + Alternative tags accounted for 90% of tags. • Over tagging was not a significant problem.

  15. Some Benefits of The Taxonomy Work • Breaks down organizational barriers • Cross-agency team worked on a common set of categories. • Related content more easily identified and linked within CMS. • Enables searching across organizations, improves search results • More inclusive search results. • Assists content managers in assembling: • New topics and sites. • Documents of interest. • What’s important today.

  16. Taxonomy Benefits (2) • Improves usability • Tagged content exponentially increases content managers’ ability to associate and present like content to the end user. • May be used to extend future Web capabilities • Faster identification and delivery of information (e.g. RSS feeds) on defined criteria. • Search and retrieval enhancements (grouping by related terms, filtering search results) • Serendipity: Discovery of new, unanticipated related information.

  17. Web Standards Boards – Organizational structure FDA Internet Improvement Team FIT Core Team Design & Editorial Board Web Tools & Applications Board Info Organization & Access Board Taxonomy Team

  18. Web Standards Boards – Membership • OIM and External Relations (Chairs) • Board members may be nominated or self-nominated, then approved by Chairs • One representative from each*: • CDER • CFSAN • CDRH • CBER • CVM • OC • ORA • NCTR • OIM • OER * Non-contract personnel only

  19. Taxonomy Team – Charter • Taxonomy Team is responsible for maintaining: • The Taxonomy, a multi-faceted classification scheme. • Team rules and procedures for change management. • Taxonomy training materials. • Taxonomy Team will consider costs and benefits of suggested changes. • Taxonomy Team will: • Manage relationships with Taxonomy change requesters. • Identify new opportunities for use of the Taxonomy across the agency to improve information management practices. • Promote awareness and use of the Taxonomy.

  20. Questions Joseph A Busch Founder & Principal Taxonomy Strategies LLC +415-377-7912 jbusch@taxonomystrategies.com www.taxonomystrategies.com

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