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Qedge Document Management Software
4 software items found
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Nonconformance detection & reporting system. Deviations management is a key role in assuring product Quality, Purity and Strength. Any non-compliance of an established GMP standard or of approved requirements, specifications and standard operating procedures (SOPs) needs to be identified, recorded and evaluated. ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
A protocol is a written statement to conduct the validation process along with the procedure, test method, equipment handling, specifications, acceptance criteria, reports and approval. Protocol management is a part of document management system in pharmaceutical and life science industries. Any official procedure or system of rules need to be ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Effective change management for better control: QEdge Change control management is a step-by-step approach to manage documented, well traceable and compliant approach to changes that take place in a system or product or process in any industry. As rightly said, “Change” is inevitable, and it is important to have ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
SOP Quality Management: 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 ...