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Qedge Xprt Software
10 software items found
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Investigation is an effective tool for identification of root cause for the potential issues observed in an organization. It ensures creation and effective management of investigation for identification of root cause. A configurable workflow design in place with defined responsibilities at each stage for speedy and effective conclusion in a time bound manner is experienced in an Investigation ...
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 validated from a base. For our industry, the base is ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Work Instructions are documents that clearly and precisely describe the correct way to perform certain tasks that may cause inconvenience or damage if not done in the established manner. These instructions are helpful in providing detailed specification tasks which are referenced in the procedure. They aid in trainings management and reduce mistakes because of step wise instruction process ...
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 ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Share and manage training data across the company. Training records management software is particularly useful for compliance in regulated markets especially in pharmaceuticals, biotechnology and healthcare domains. Each time SOP or Work Instruction is revised it automatically identifies which are end consumers and notify them as well as their training managers. Auto alert also get generated in ...
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 robust change management process across the organization for process ...
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. Any critical or major deviation which affect the product quality, reliability of ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
eLearning management software (lms) solution as a part of QEdge, is an excellent enterprise tool for learning management and continuous learning across the organization. The content for eLearning can be organized for multiple location, multiple department and access rights can be controlled and managed based on department and organization. eLearning management software (lms) is also backed with ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Better control of inspection & assessment: Auditing is a crucial job within a pharmaceutical company. The purpose of carrying out a GMP audit in the life sciences Industry is to verify compliance with the principles of Good Manufacturing Practices and to recommend any necessary corrective actions. The breaches identified in the audit check list help the management to review the quality system ...
by:Sarjen Systems Pvt. Ltd. based inAhmedabad, INDIA
Pharmaceutical companies are required to submit a full Product Quality Review (PQR) or APQR in the U.S. and PQR in Europe to government health authorities annually, detailing key aspects of the manufacturing process for each drug they produce. APQR or PQR is a mandatory requirement that used to verify the consistency and appropriateness of an existing manufacturing process. It plays a critical ...