Meeting Regulatory Requirements
We realized that addressing regulatory requirements across the regions in which we operate was taking more and more time and resources, and wanted a way to streamline those activities. And we selected Scigeniq’s RMS not just for its capabilities, but because of their position as a leading software vendor for pharma companies in the MENA region. Ayman Cheikh-Lahlou, CEO of Cooper Pharma
A Full Suite of Solutions For Small to Mid-Sized Pharma
Get the help you need with quality, regulatory, manufacturing, and content-management processes.
Quality Management
Manage 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.
Document Management
Get 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.
Regulatory Management
Manage regulatory information including communications, deadlines and dossiers is critical to ensuring accurate and timely submissions. The RMS acts as a central point of management while ensuring transparency and compliance.
Electronic Batch Records
Automate batch record management, save time, improve accuracy, and ensure compliance with regulatory requirements. EBR allows the integration of devices and equipment and collects information throughout the manufacturing process.
Training Management
Automate the critical tasks of tracking, planning, and completing training for every team member. Centralize your program, simplify compliance, and ensure your workforce is always prepared, even during rapid expansion.
Asset Management
Track and manage their critical physical and digital assets used in research, development, and production. Integration with Scigeniq Quality Management System (QMS) further streamlines operations.
A True Partner for All Your Operations Needs
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
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.
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Once a month we share information, insights, and news related to the Life Sciences industry, with a focus on strategies and technologies for operational efficiency in document, quality, regulatory, training, and manufacturing processes.