Biotechnology - , ,
Enterprise Compliance Solution for Regulated Businesses Comprehensive Software Platform for Maintaining 21CFR cGMP Compliance Across Pharmaceutical Environments. Uniting QA Systems, Time Tracking, Documentation, Training, CAPAs, Real Time Laboratory and Batch Data Entry/Capture, Results, Reports and more. All in a single, seamless platform. The Arch System unifies the individual aspects of your quality management systems (QMS) into one completely integrated regulatory software platform. Method SOPs, training, CAPAs, electronic files, data management and more. No more individual or unrelated software programs to manage your compliance. Encompassing quality assurance (QA) and quality control (QC) environments for a cohesive and streamlined relationship. Project and compliance details are captured and maintained in real time and managed comprehensively. Our proprietary electronic worksheet method generation feature is unique. It allows for actual real time SOP execution directly into the tablet. Within your quality control environments these entries are checked for accuracy immediately, based on the parameters specified in the SOP being performed. Inhibiting mistakes before being able to proceed, assuring total quality and saving time. Now the separate elements of the project are tracked comprehensively, in actual real time. Starting from project initiation, a precise time tracking feature is enabled.From beginning to end, encompassing document creation, method development, routine analysis, reviews, reports, inventory and beyond. Know exactly how your resources are being used. Significantly assisting project management timelines, goals and resource allocation. Communication, turnaround times, inventory and resource management are greatly enhanced. Saving your business time, costly mistakes, repeat procedures and insuring your compliance for governmental agencies.
reCAPTCHA
Apache
WordPress.org
Google Font API
Google Cloud Hosting
YouTube