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  • Home
  • Solutions
    • Quality Processes
      • Change Control
      • Deviation
      • Investigation
      • CAPA Management Software
      • Market Complaint
      • OOS and OOT
      • Pharmacopeial Change Control
    • Document Control
      • SOP
      • Protocol
      • Work Instruction
      • Specification
      • Controlled Copy Release (Doc Issuance)
    • Learning Management System
    • Product Quality Review (PQR)
    • Vendor Qualification
    • Ready-to-deploy QMS
  • Resources
    • Blogs
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    • Use Case
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Document Management System

document
Document Management System
Are You Controlling Your Documents or Are Your Documents Controlling You?

In the pharmaceutical industry, where precision, safety, and compliance are non-negotiable, proper document management is critical. From production records and SOPs to compliance documents, every piece of information plays a vital role in ensuring regulatory adherence and product quality. However, […]

by QEdge Team

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October 3, 2024
Simplify Pharma Document Management with QEdge A Complete Solution for All Your Needs 
Document Management System
Simplify Pharma Document Management with QEdge: A Complete Solution for All Your Needs 

Managing documents in the pharmaceutical industry is a complex and critical task. From creation to archival, every document goes through a lifecycle that requires careful handling and strict compliance with regulatory standards. Whether it’s checklists, logbooks, data sheets, or batch […]

by QEdge Team

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September 6, 2024
Unlocking Excellence in Pharma Manufacturing with the Best APQR Software
Document Management System  ·  QMS
Unlocking Excellence in Pharma Manufacturing with the Best APQR Software

In the pharmaceutical industry, keeping your product quality consistent and meeting regulatory standards is essential. The Annual Product Quality Review (APQR) plays a key role in helping you achieve this. By leveraging the best APQR software, you can streamline this […]

by QEdge Team

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September 5, 2024
Automation help preparing APQR
Document Management System
How can Automation help preparing APQR in one day?

What is PQR or APQR in pharma? Annual Product Quality Review or Product Quality Review  can be identified as a manoeuvring and compilation of data from various dimensions involved in product manufacturing to display the quality of product. It includes […]

by QEdge Team

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September 27, 2022
Document Management System (DMS) at a Glance
Document Management System
Document Management System (DMS) at a Glance

A Document Management System (DMS) is a system used to track, manage and store documents and reduce paper. Most can keep a record of the various versions created and modified by different users. QEdge DMS at a Glance QEdge DMS provides the features and functions […]

by QEdge Team

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July 12, 2017


QEdge Quality Management Software Suite

  • Quality Processes - QMS
  • Document Management - DMS
  • Training Management - TMS/ LMS
  • Product Review - APQR/ PQR
  • Vendor Qualification
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6th Floor, Arista, 100 Feet Anand Nagar Rd, Jodhpur Village, Ahmedabad, Gujarat 380015
Phone : +91-79-66214899

Email:  sarjen@sarjen.com

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