The Essential Foundational Investment for any GMP Program is an EAM System. Before implementing other quality systems like a Quality Management System (QMS) or a Manufacturing Execution System (MES), your […]
By: Lisa Bowman, Executive Director of People, Culture and Community In the near future, the American workforce is poised for a significant shift as the baby boomer generation, a substantial […]
This article explains 21 CFR Part 11 and EU Annex 11 regulations for electronic records and signatures in GMP-regulated activities. It covers compliance requirements, benefits, and differences between Part 11 […]
As the Life Sciences industry is being driven by corporate M&A, it is essential that organizations effectively leverage enterprise asset management systems (EAM) to meet industry pressures that stem from […]
The productivity benefits of implementing an EAM system early when building a new facility provide immediate return on investment for an organization. Some of the benefits include paperless document routing […]
If you enter the phrase “How often should we upgrade software?” into a search engine, the results are likely to come back in one of two ways: Stay current, update […]
In the previous blog in our Battling the Mandate Series: Successful Solutions for ERP / EAM Interaction, we discussed common integration methods as well as described the difference between the […]
Now that we’ve laid the foundation for why an organization can gain higher return on investment by using a purpose-built EAM / CMMS rather than an ERP module, I want […]
In the previous blog, I discussed the importance of using purpose-built software. Because we are a purpose-built EAM solution provider, we see many Life Sciences companies moving away from generic […]
So now that we have discussed the top considerations when implementing a multisite software solution, we are going to cover the benefits and the overall impact on the organization as […]
