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This Industry ready solution for Pharma & Life Science is a GxP compliant enterprise wide quality management system that configures all the quality events on a single platform. It provides high level of flexibility of configuration according to individual business scenario. With an experience of more than 25 years of workflows in the industry, and the mix of technology expertise, Sarjen has developed the right systems to edge out your quality management hassles.
Celebrating 25 Years of Trusted Partnerships
QEdge eQMS solution helps organizations to manage their QMS process with poise. It brings all the quality documents like market complaints, investigation, CAPA, deviation, risk assessment, OOS, OOT change control and many more on a single platform.
QEdge DMS ensures that documents such as manuals, SOPs, work instructions, specifications, BMRs are managed and retrieved efficiently. It also helps tracking document distribution, retrieval and maintaining records of distributed copy.
QEdge PQR offers automation and digitization ensuring data integrity. It is compliant with all major standards including 21 CFR PART 11 and EU Annex 11 Standards.
QEdge VQM assures that materials procured are produced, packaged, and shipped under a controlled process that results in consistent quality conformance and meets regulatory expectations.
Excellent in terms of regulatory compliance for example 21 cfr part 11, EU, MHRA, Brazil etc. It gives great comfort to regulatory auditors in terms of compliance.
Easy to use. You can train any person without any difficulties
We customized QEdge as per our company requirement. So that process flow did work exactly same as per our defined procedure.