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Good Products has announced it will hold its Electronic Document Management (EDM) Summit at IBM House, the Southbank, London, UK on 24 November 2009.

This first summit will discuss regulatory compliance using Microsoft Office Sharepoint Server 2007 and provide an overview on organising document management to comply with electronic common technical document (ECTD) and good manufacturing practice (GMP) guidelines.

Speakers will include Pfizer, Adlib, Thomas Reuters and ARX.

The biopharmaceutical sector is challenged with stringent requirements for the management and submission of electronic documents.

The growing need for e-submission capability coupled with more open platform document-management options are creating new opportunities for creating value through increased efficiency.

This half-day summit hosted by Good Products is aimed at chief executive officers, IT directors, document-management specialists and regulatory, quality and clinical managers.

The informative session will provide attendees with a detailed overview of current best practices for regulatory compliant document management.

Independent industry experts will give presentations on common practices, agency expectations for submission-related content and the compliant management of documents and content.

The summit will demonstrate how best-of-breed solutions from different vendors can be integrated effectively to create user-friendly solutions for document management within biopharmaceutical research and development and manufacturing.

For more details and to register, visit the company website.

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