How to achieve industry compliance within a highly regulated setting

Discover how a large UK pharmaceuticals manufacturer improved its data quality and real time reporting capabilities, as well as remaining compliant within a highly regulated industry

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Pharmaceutical Manufacturing:
Enterprise Asset Management Within a Highly Regulated Industry

(This event has past - Tues Jan 26, 2021, 2:00 PM GMT)

You can still watch the webinar by clicking here
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BPD Zenith - Explore some of the industry challenges faced by a large UK pharmaceuticals manufacturer in choosing to upgrade their IBM Maximo EAM solution. This included functionality for mobility, calibration and enhanced reporting - all within a strictly regulated and certified industry.   Find out how this led to a reduction of 40% in unplanned work in just 6 months!

We explore the importance of data quality from its input source, through to live enhanced reporting, and how this was implemented as part of a business-critical upgrade.

Join BPD Zenith to discover: 
  • Modern EAM System Benefits

  • Creating an Optimised Mobile Workforce

  • Calibration

  • Business Intelligence Reporting

  • 40% Reduction of Unplanned Work in just 6 months!

  • Delivered on time and within budget

More from BPD about the project...

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This paper outlines important strategic considerations for implementing asset
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A Complete Life Sciences Solution

Employ a single-vendor solution that offers a risk-based approach for asset management to address Food and Drug Administration (FDA) regulations, including Good Manufacturing Practices (GMP) and FDA 21 CFR Part 11