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Life Sciences
Quality is at the heart of Life Sciences organizations
Quality is at the heart of the highly regulated Life Sciences industry. Ever changing regulations and technology are improving the…
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Services
Document collaboration with contractors, suppliers and owner/operators
Online collaboration is the key accelerator in Capital Projects. It must be used in a clever way otherwise there is…
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Life Sciences
Paperless validation for Life Sciences projects
Pharmaceutical organizations in the life sciences industry face challenges in developing and maintaining data integrity due to complex validation documentation.…
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Services
Effective engineering document management lies at the heart of successful construction and capital projects
Effective document management is key to ensuring successful construction and capital projects. From initial design documents, to work orders, to…
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Services
Tracking engineering documents in capital projects
In my last blog in this series on Engineering Document Management for capital projects I discussed the importance of a…
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Automotive
Learn how project workspaces are essential to keep an engineering capital project on track
Work-in-progress documents are managed in project workspaces. Project members are assigned to roles and project tasks are assigned to project…
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Services
Understanding the Master Document Register within an engineering capital project
My last blog in this series on Engineering Document Management in capital projects discussed a best practice deployment of OpenText™…
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Services
Making the best out of your Engineering Document Management implementation
Opentext™ Extended ECM for Engineering is one of the most comprehensive engineering and asset information management platforms available for engineering,…
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Services
Learning Management Systems and Life Sciences Quality & Manufacturing solutions – better together!
OpenText™ Documentum™ for Quality & Manufacturing (Q&M) solutions are widely used in Life Sciences companies to create, maintain, and revise…
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Services
How prepared are you for the EU MDR?
On May 26, 2020, the EU Medical Device Regulation (MDR) exited its transition period. There are still questions about how…
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