1. Spring 2008: features & functionality overview Julie Gordon, Product Director Presented at SLA DPHT Spring Meeting, St Petersburg, Florida

2. What does Inteleos include? Launched in May 2006 10,000+ brand drug records –16,400+ indications –70% in active development Previewing at SLA PHT –9000+ US generic drugs –New design –Improved search capabilities –Expanded content

3. Brand drug coverage Preclinical > launch > post marketing, includes associated licensing activity Comprehensive FDA submission & approval filings Competitor profile Tracking advancements in technological innovations: –bio-specific antibodies –modified release mechanisms –gene therapy Detailed clinical trial coverage – summarized per drug record including links to ClinicalTrials.gov Full-text archive of selected articles from The Pink Sheet and links to related press releases

5. Straight to the information Search & filter features, including: –Product type, method of delivery –Discontinued by phase –Development timelines Flexible reporting –Analysis of data in graphical or chart displays –Multi-format exporting –Save search results –Share content with colleagues online Update alert –Keywords & search queries

8. Injection - intravenous, 10mg/ml

9. COMPARISON ANALYSIS PIPELINE MATRIX

11. Whats new? New design Improved usability –Full Boolean searching –Drug name instead of brand/generic/code –Better organization of search and analysis pages Searchable development timelines Pharmacokinetic data for FDA approved drugs LINKING TO GENERIC DRUGS Searchable EMEA submission and approval details

13. Generics coverage FDA tentative approvals and approved generics Links back to brand drugs Continuous updates of FDA Drug Master Files Full indication coverage Identification of generic equivalencies Orange Book approved dosage forms To Come: –linked and searchable Paragraph IV data –selected articles from The Pink Sheet

15. SCREEN SHOTS –DMF files filter option export option

16. Inteleos Seamless linking between brand and generic drugs Comprehensive and searchable FDA and EMEA submission/approval details Tracking drug and biologic development Flexible search and export options Dynamic analysis tools

17. Thank you For more information please visit our booth