Dell EMC, a leader in enterprise content management solutions, has announced Suite, a unique product suite within EMC Documentum for Life Science for enterprises who operate in both the pharmaceutical and medical device industries. Suite provides clinical, regulatory, and design history file/device master record document features to fully enhance the lifecycle of products from design to manufacturing. Not only is it compliant with industry regulations, its use is efficient and includes quality control features that greatly assist in product trials. eTMF capabilities are enhanced as well, giving you a detailed view of your data with support for both 2.0 and 3.0 DIA eTMF Reference Models. And, development of new products couldn't be easier with a R&D inventory to speed regulatory submissions and compliance.
Suite is comprised of four complementary solutions:
- Electronic trial master file (eTMF)
- Research and development (R&D)
- Submission store and view
- Quality and manufacturing (Q&M)
Suite is designed to improve efficiency, user experience, and visibility of critical information across the enterprise. Says Andy Crowne, Vice President of Industry Solutions and InfoArchive: “Many Life Science organizations have difficulty implementing a cohesive solution for both pharmaceutical and medical device documentation, since available systems are often too complex or cost-prohibitive for smaller businesses. EMC Documentum for Life Sciences solution suite brings both options together in a single repository, giving companies of all sizes the choice and flexibility of implementing a single medical device solution or deploying R&D and Q&M independently to align with business functional areas.”
Read more about Suite on Dell EMC's press release
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