Webinar: Quality Management as a Competitive Advantage
During this session, we discussed the transformative role that a modern Quality Management System can play in mid-size pharma companies. We looked at the key capabilities of a modern QMS and what to look for when evaluating alternative QMS systems. We also showed how Scigeniq’s QMS creates a fully-documented, closed-loop quality cycle from the initial issue or deviation right through to documented change control.
Watch on DemandScigeniq™ QMS
Our Quality Management system manages every step in the quality process, from deviation to CAPA to change control. The result is that the entire end-to-end process is managed, documented, and ready for inspection.
Scigeniq ™ DMS
Our Document Management System provides a complete set of functions including version control, access control, and workflows for review, approval, and change management. All in an easy-to-use environment that meets all regulatory requirements.
Scigeniq ™ RMS
Managing regulatory information including communications, deadlines and dossiers is critical to ensuring accurate and timely submissions. Our RMS acts as a central point of management while ensuring transparency and compliance.
Scigeniq, Your Partner of Choice
A Team of Experts
Our team has extraordinary knowledge of every aspect of the quality, regulatory, and document management processes in use across the life sciences industry. We bring that expertise and know-how to every customer through the combination of our expert services and our software solutions.
More Than Software
Scigeniq software applications encapsulate proven processes and practices used by industry leaders. Our process expertise is “built-in”, so when you adopt Scigeniq solutions, you are implementing proven best practices at the same time.
End-to-End Capabilities
Scigeniq has a full suite of quality, training, document management, and regulatory solutions. That means that end-to-end processes can be optimized and automated to deliver maximum impact.