CASE STUDIES :
Office Central de la Pharmacie
Office Central de la Pharmacie

Diadeis Mission
OCP (Office Central de la Pharmacie) is France's biggest pharmaceutical dispatcher with 40.5% of the market. It has 8 regional platforms and 59 dispatch centres. It distributes 24,500 standard products, making 4 million products in all. <dernière phrase effacée>
DIADEIS has developed the editorial system and document database for use on a variety of media (CLICKADOC system)

The main DIADEIS mission is the monthly updating, design, duplication, and routing of CD-ROMs. DIADEIS also carries out the page layout for "Dico Plus" (OCP's yearly printed reference catalogue) using automated composition. DIADEIS is also involved in the evolution of the CD-ROM features.

Process
Monthly CD-ROM production process:
• Receipt of new data for updating the CLICKADOC CD-ROM
• Verification of data integrity
• Processing of data for incorporation into CD-ROM
• Production and validation of Worm
• Duplication of CD-ROMS
• Routing of CD-ROMS

Technology
• ORACLE V8i database / Intermedia
• Production of generic APIs for developing web interfaces for the application
• XML entry of product data sheets
• XML extraction of product data sheets for the CD-ROM
• Production of the CD-ROM using DIADEIS technology
• CDBL
• DICOPLUS book composed with CCI and QuarkXpress

Human resources
• One project leader
• Two development engineers
• One data entry operator (CD-ROM)
• A DTP team

Volume
• 11,000 CD-ROMs produced each month
• 300,000 product data sheets (medication and nonprescribed products)
• Composition of 1,900 pages for DICOPLUS

Main challenge
Enable real time updating of the customer's Web site and shorten the delivery time of CD-ROMS to the OCP customers' dispensaries.

Input
XML product data sheets.
Output
Monthly production of product data search CD-ROM and yearly production of the printed DICOPLUS publication.

Result
OCP has the biggest pharmaceutical products database in Europe that can be accessed by extranet (5, 500 dispensary subscribers), with the added feature of managing foreign equivalents (equivalent products) and managing drug contraindications.
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