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Audit Management Software
11 software items found
by:Honeywell | Life Sciences based inHamilton, NEW JERSEY (USA)
Medical device manufacturers must comply with 21 CFR Part 820, medical device reporting (MDR), premarket notification 510-(k), investigational device exemption, and quality system (QS) regulations. Audits help manufacturers to improve quality, lower costs, and increase compliance. But, managing them manually can become a time and resource intensive ...
by:2KMM Sp. z o.o. based inKatowice, POLAND
GoResearch is a fully validated, innovative internet platform for electronic data capture(EDC) created by 2KMM for research projects such as clinical/observational studies andpatients ...
by:CRScube Inc. based inSeoul, SOUTH KOREA
In the paperless era, the clinical trial industry is changing. Until now, the Trial Master File (TMF) has consisted of traditional paper documents, images, or media organized in a binder stored in file cabinets. In accordance with FDA's CFR 21 Part 11, we have developed cubeTMF to provide a validated system for a cohesive workflow for a truly paperless clinical trial. cubeTMF® streamlines the ...
Manufactured by:Voyager Imaging a division of Intellirad Solutions Pty Ltd based inEast Hawthorn, AUSTRALIA
Image and Report distribution to Referring Clinicians and Specialists is the overarching requirement for the finalisation of the diagnostic process. Voyager Imaging provides several mechanisms for the provision of reports and image ...
by:Endpoint Clinical based inWakefield, MASSACHUSETTS (USA)
Building your IRT system on PULSE allows you to take back control of complex processes. The reporting and messaging functionality helps stakeholders perform day-to-day tasks more efficiently and ...
by:ComplianceQuest (CQ) based inTampa, FLORIDA (USA)
Empower your employees with real use cases for AI in quality and safety management that improve efficiency, decrease errors, and free up resources. ...
by:DrPro based inSurat, INDIA
Use DrPro's Medical Billing Solutions to Improve healthcare. Optimize processes, reduce mistakes, and improve the handling of finances to help make things less stressful for ...
by:BC Platforms based inZürich, SWITZERLAND
BC | INSIGHT is a data and research management solution for clinical genomics studies. Genomic and phenotypic data is collected and stored on the platform, and users have access to data and tools through an application account. All common data types for NGS, GWAS, variant analysis, linkage, and other statistics can be managed on the platform. ...
by:Endpoint Clinical based inWakefield, MASSACHUSETTS (USA)
DRIVE: Clinical Supply Management Solution. An enterprise-level solution, DRIVE, enables you to manage clinical supplies at the sponsor, depot, and site levels, providing your team with full visibility and traceability of inventory across all trials, inclusive or exclusive of the use of an ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
Document change control software is essential for ensuring compliance and managing change in regulated industries such as life sciences and manufacturing. By utilizing this software, companies can effectively address the complexity of change control and streamline their ...
by:AWS Truepower, LLC based inAlbany, NEW YORK (USA)
Discover how our validated, FDA CFR Part 11 compliance training management system helps you comply with evolving FDA Regulations. Keep your workforce up to date. Medical device and pharmaceutical manufacturers trying to keep up with ever-changing regulations have a tough job. Medical technology advances quickly, and with it the need for compliance systems to support patient safety. To help you ...