FDA Inspection Fiscal Year (FY) 2023 Annual Report: Top 3 Citation Categories Related To Drugs
We analyzed the drug-related citations in the Fiscal Year (FY) 2023 Annual Report from the Office of Compliance paying specific attention to the broader examination of initiatives such as inspections, quality control, and adherence to Good Manufacturing Practice (GMP) standards.
Download the report to learn what we found.downloAD THE REPORT
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 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.
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.