Managing Regulatory Submissions with SharePoint: Connecting the Process from Authoring to Submission

ONLY TWO DATES REMAINING

Please join us for the next event in the NextDocs Compliance Without Complexity Seminar Series at a Microsoft Office near you!  >>REGISTER NOW for Chicago or Raleigh<<

Date Microsoft Location
May 20 Boston Area (Waltham, MA)
May 21 Iselin, NJ
May 27 Malvern, PA
June 1 San Francisco
June 3 San Diego
June 10 Chicago
June 17 Raleigh

The Challenge:

Regulated documents are typically housed in one system while they are being compiled, and another as they are prepared for publishing and submission. Each system brings its own user interface and data model, and the result is that organization usually have to invest substantially in integration and customization efforts to connect systems and integrate the process. The result is high complexity and the high cost that always accompanies high complexity.

The Solution:

With an integrated solution working from a single set of documents, the entire process can be simplified and accelerated. And with the DIA leading a push for a new reference model that ensures common structures and properties for R&D documents, there is now the potential to implement a complete, end-to-end process without data transformation and system integration challenges.

During this Session:

  • You will see a SharePoint-based, end-to-end solution that takes documents from initial authoring and review to publishing
  • You will learn how a SharePoint-based solution for managing regulatory documents can dramatically reduce complexity and associated cost
  • You will hear how the DIA Reference Model is being put into action in the NextDocs Regulatory Documents solution

Agenda:

Time Topic
8:30 – 9:00 Registration and Breakfast
9:00 – 9:15 Microsoft in Life Sciences
9:15 – 10:00 The Current and Future State of Regulatory Submissions
10:00 – 10:10 Break
10:10 – 11:40 Drama in Real Life: An End-to-End Solution for Managing Regulatory Documents from Authoring to Submission
11:40 – 12:00 Question and Answer
12:00 – 12:30 Lunch
12:30 – 1:30
(Optional Session)
Case Study – Implementing an Integrated Solution for Managing Regulatory Documents

To register, please complete the form below. Seating is limited, so register TODAY.

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