Serán BioScience customized their QMS with Novunex

//Serán BioScience customized their QMS with Novunex

Serán BioScience

Serán BioScience, Inc., located in Bend, Oregon, USA, provides optimized drug development and manufacturing services. The laboratory supports the development of pharmaceuticals in early stages with analytical methods, assisting in performance evaluation and creating the foundation for clinical manufacturing testing.

Q: What did you find as a result of buying Novunex eQMS?

A: The staff at Novunex are very easy to work with and were able to customize the software to fit our unique company needs.

Q: What specific feature did you like most about Novunex eQMS?

A: The dashboards offer excellent visual ques to users when training is due, or a document is pending approval.  The simple layout allows users to easily maneuver through the system and specific process step they are assigned.

Q: What are three other benefits of Novunex eQMS?

A: First of all, the system is very flexible, and encompasses all manufacturing quality processes above and beyond the standard document control offerings. From material ordering, receipt, and testing, through the product manufacture and release, to equipment maintenance and investigation management, Novunex is a one-stop software for all quality system management needs.

Second, the system can be used to create and revise documents, as well as retain completed records. This helps our company eliminate the need for paper records, and saves us significant time and money.

And last but not least, the software developers are always looking to improve the software, and offer excellent support throughout the validation and on-going use of the system.

Q: Would you recommend Novunex eQMS? If so, why?

A: Yes, the customer support is unmatched in the eQMS industy.

By | 2018-04-05T06:22:18+00:00 March 14th, 2018|Categories: Success Stories|Tags: , , |Comments Off on Serán BioScience customized their QMS with Novunex

About the Author:

Theresa Gangloff
Theresa works as a Medical Regulatory Engineer. She has years of experience in leading SCM and QMS projects in highly regulated environments. She is facilitating design sessions with customers in the medical device manufacturing and automotive industry to define solutions and delivering outstanding systems.