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Edgewater Fullscope Blog

2 Reasons Why Pharmaceutical Companies Need to Invest in ERP

Jun 27, 2018 7:00 AM

For many large pharmaceutical companies the struggle lies in end-to-end visibility throughout an organization. When visibility throughout an organization is siloed, out-of-date or unclear to those searching, maintaining product information and handling recalls becomes cumbersome and often times can result in noncompliance fees, wasted products and millions of dollars in damage to a company’s bottom line.

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Data Integrity— A stepping stone to GMP Compliance for Pharma Manufacturers

Mar 9, 2018 7:00 AM

What exactly is data integrity? To a pharmaceutical manufacturer, it’s everything. Reporting requirements mandated by the FDA play a major role in what’s expected of a company and conscientious companies are taking it seriously. 

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Put Down the Pencil — A Modern Solution for Batch Records

Feb 26, 2018 7:00 AM

Maintaining consumer safety — the utmost important factor that keeps a pharmaceutical business afloat. This factor is the reason pharmaceutical manufacturing companies undergo strict regulations and assessments to ensure compliance and quality. If you’re someone involved in this industry then you understand the challenges of gathering information for every batch of product that’s produced.

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Webinar: Automated Validation Testing of Dynamics 365

Sep 17, 2017 8:00 PM

Although today’s Dynamics 365 for Finance and Operations ERP system has achieved significant technological advances, validation is still conducted by many today as a very manual process. In this session, we will take a deep dive into the principles of lean validation testing and discuss how you can fully automate the Dynamics 365 validation process. We will explore automated requirements management and test script linking, automated validation test script capture and execution, electronic document route/review/approval, automated risk management and much more. You will not want to miss this event if you are seeking to deploy Dynamics 365—or already have deployed the system and seek to maintain the validated state.

Join us on Wednesday, September 20 at 1:00 PM EST for the conclusion of our cloud validation webcast series, Automated Validation Testing of Dynamics 365, where we will cover validation planning, strategies and best practices. If you're unable to join us at that time, go ahead and register—we'll send you a recording of the webcast after the call. 

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Introducing Microsoft Dynamics 365

Dec 1, 2016 7:00 PM

By Marielena Zajac, Marketing Specialist

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Fullscope EDGE for AX Achieves Technology Evaluation Centers (TEC) Certification Status

Nov 10, 2015 7:00 PM

Fullscope EDGE for AX is now certified by Technology Evaluation Centers (TEC), a leading provider of independent software research, evaluation tools and selection services. EDGE for AX completed the certification program which included a scripted product demonstration session and benchmarking analysis with a TEC research analyst.

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Without a trace.....

Jan 1, 2014 7:00 PM


In earlier posts
here and
here, we talked about how social media is changing the game when it comes to consumer recalls. I just took a peek at the FDA enforcement report in my inbox, and all I can say is that it will help motivate my January diet resolutions… Today, let’s take a look at another key part of the recall readiness toolkit: traceability. Over on
FoodDive, the
Traceability playbook describes six key advantages of implementing a comprehensive, modern traceability system:
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A Help or Hindrance: Is Your ERP System Built for Your Industry? Part 2

Dec 16, 2013 7:00 PM

Part Two: Manufacturing Processes & Production Requirements

Batch processing is one of the simplest manufacturing processes. In some cases, companies using discrete ERP applications to run their businesses are forced to use work-arounds to solve process issues. In batch processing, the company can use either a bill of materials or a formula. However, discrete BOM-based applications have limitations, including units of measure (UOM), material/routing relationships, variable consumption, percentage-based formulations, step consumption, variable output and unplanned co- and by-products.

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