Edgewater Fullscope Announces New Series of Industry Solutions for Manufacturers

Edgewater Fullscope Announces New Series of Industry Solutions for

First Fullscope EDGE Industry Solution Aimed at Life Sciences and
Pharmaceutical Manufacturers

NEW ORLEANS, March 18, 2013 (GLOBE NEWSWIRE) -- Convergence 2013 -- Edgewater
Fullscope, Inc., a wholly-owned subsidiary of Edgewater Technology, Inc.
(Nasdaq:EDGW) (http://www.edgewater.com), today announced a new series of
industry solutions designed to extend existing functionality in Microsoft
Dynamics AX 2012 enterprise resource planning (ERP) for chemical, life
sciences, pharmaceutical, food and consumer product goods (CPG) manufacturers.

The first product, Fullscope EDGE for Life Sciences & Pharma, will help
address core issues that life sciences and pharmaceutical manufacturers face
to help them meet the U.S. Food and Drug Administration's (FDA) Quality System
Regulation 21 CFR Part 11, cGMP and other various regulatory and international
standards such as ISO and Six Sigma. Features will include:

  *Corrective Actions & Preventive Actions (CAPA), allows users to automate
    processes, including capturing an issue, determining the root cause and a
    corrective or preventative action plan, verifying and validating the
    action plan and tracking for resolution.
  *Electronic device history records (eDHR), helps reduce significant storage
    requirements and quality issues caused by paper records.
  *Electronic device master records (eDMR) and Electronic master batch record
    (eMBR), enables companies to completely compile and track all records
    about a medical device or production lot.
  *Enhanced eSignatures, includes dual forms of identity and certificate
    aging to help ensure life sciences and pharmaceutical companies can adhere
    to the strict interpretation of FDA 21 CFR Part 11.
  *Flexible/skip lot sampling plans, enables companies to inspect a fraction
    of a lot and realize reduced quality and material handling costs, faster
    material throughput and less redundant and destructive testing.
  *Approved customer lists, especially important when dealing with controlled
    substances and branded products, offers control over what products a given
    customer can buy and when they can buy them.
  *Vendor scorecards/vendor qualification reporting, provides the ability to
    rate vendors based on their delivery, quality, cost and consistency.
  *Validation requirements, includes a toolkit to help life sciences and
    pharmaceutical companies meet FDA compliance requirements.

"Life sciences and pharmaceutical manufacturers face strict FDA and other
compliance requirements and must have regulated procedures and supporting
documentation," said John Scandar, senior vice president of Edgewater
Fullscope. "Microsoft Dynamics AX has robust functionality to solve most of
this industry's business challenges. EDGE for Life Sciences & Pharma provides
a cost effective, easy to use solution to meet some of the deeper compliance

Fullscope EDGE for Life Sciences & Pharma will be available in the second
quarter of 2013.

About Edgewater Fullscope

Edgewater Fullscope is an award-winning Microsoft partner and one of the
largest resellers of Microsoft Dynamics AX enterprise resource planning (ERP)
software and services in the United States and Canada. Its customers include
discrete, mixed mode and process manufacturers. Fullscopealso offers software
and implementation services for Microsoft Dynamics CRM, SharePoint and
Business Intelligence.For more information, visit www.fullscope.com.

Product or service names mentioned herein may be the trademarks of their
respective owner.

The Edgewater Technology logo is available at

CONTACT: Company Contact:
         Timothy R. Oakes, Chief Financial Officer
         Russell Smith, Senior Vice President/Investor Relations
         Tel 781-246-3343
         Investor Relations:
         Cody Slach, Liolios Group, Tel 949-574-3860, EDGW@liolios.com

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