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QEdge makes it easy to automate your SOP process and workflow with better time management and resource allocations.
QEdge SOP management software offers a system to track SOPs and manage SOP life cycle that includes creation, review, approval and release along with distribution with unique distribution code and achieving. With every process flow, the associated access rights ensure the users to works on tasks defines for them for effective process control.
A Standard Operating Procedure (SOP) is a set of instructions that describes all the relevant steps and activities of a process or procedure. An SOP is a procedure specific to your operation that describes the activities necessary to complete tasks in accordance with industry regulations, provincial laws or even just your own standards for running your business.
In Pharmaceutical and Life Science Industry, Standard Operating Procedure (SOP) is a tested, verified, approved, and documented way of executing operations that form the pharmaceutical industry’s basis. It provides step-by-step guidance for the personnel to perform a specific process.
Every process, procedure and operation have its SOP that is regulatory compliant that helps them to be executed or initiated without its SOP. Let us go through a few points on why SOP quality management is important.
QEdge is an enterprise-wide quality management software system that helps manage quality process at all stages of business.
Managing SOP’s digitally challenges like unsigned SOPs, outdated SOPs and incomplete SOPs. QEdge Pharmaceutical QMS software streamlines the data collection processes and assures that each data point is considered. Our system automates SOP management processes such as data collection, task assignments, scheduling, follow-ups, as well as creation, review, approval, and escalation of document-based processes. It sends notifications and/or reminders for training when new SOPs are released and become part of the process in your pharmaceutical organization. With our solution, you can easily track SOP’s, trace revisions and record all data for audit purposes.