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Streamline Software Implementations for Medical Device Companies

August 2, 2017

At Mobius Logic, we understand the challenges that face your IT, Regulatory & Compliance, and Logistics Applications departments to stay compliant with FDA regulations and react to FDA Warnings especially when it comes to ensuring your software application conform to your quality standards. For this purpose we put together a holistic approach to Risk Management for the Life Sciences Industry. Instead of juggling between your QA, Regulatory Consultants and IT Vendors, we have a single team that can do it all.

 

 Our teams are well versed in the CAPA methodologies of life science companies and have completed several successful implementation under strict guidelines governed by IQ/OQ procedures. By having risk mitigation and risk management experts being part of our software development teams, we simplify your task of having to coordinate between several vendors and consultant to get a successful implementation that is on-time and on-budget. 

 

If you have received an FDA warning regarding one of your IT systems or applications, or are contemplating automating some of your business procedure using IT systems and application, Contact Us, to help you plan it out and deliver a successful result.

 

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