Transforming Industry Standards with Innovative Technology
At FidNos Corporation, we specialize in delivering state-of-the-art software solutions tailored to the pharmaceutical and food industries. Our cutting-edge technology is designed to streamline operations, ensure compliance, and drive innovation, helping you stay ahead in a rapidly evolving marketplace.
Most of our software is fully compliant with FDA regulations, including 21 CFR Part 11, 21 CFR Part 111, 21 CFR Parts 210-211, 21 CFR Part 606, 21 CFR Part 820, and 21 CFR Parts 1270-1271. Additionally, we adhere to OSHA and EPA regulations, such as 29 CFR for Occupational Health and 40 CFR for EPA standards. For our European clients, our solutions comply with EU Annex 11 and GDPR.
Document Management System (DMS)
Document Management System (DMS) helps businesses achieve a paperless Quality Management System (QMS) while ensuring compliance with CFR and EU Annex 11 regulations. With powerful automation, version control, and secure access, your organization can streamline document workflows and maintain regulatory compliance effortlessly.
Quality Management System (DMS)
Quality Management System (QMS) helps businesses achieve a paperless Quality Management System (QMS) while ensuring compliance with CFR and EU Annex 11 regulations. With powerful automation, version control, and secure access, your organization can streamline quality workflows and maintain regulatory compliance effortlessly.
Computerized Maintenance Management System (CMMS)
In situations where downtime and equipment failure can have severe consequences, implementing CMMS becomes crucial. CMMS will help you manage and track maintenance tasks, including assets management, work orders, preventive maintenance, parts/vendor management, and downtime in real-time.