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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
    • Case Studies
    • Use Case
  • About us
  • Contact us

  • 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
    • Case Studies
    • Use Case
  • About us
  • Contact us

Blogs

Read our quality management blogs and explore more about the latest trends

Dynamic opportunity of business continuity plan through Cloud based Doc Control
QMS
Dynamic opportunity of business continuity plan through Cloud based Doc Control

Regulatory documentation is an essential part of every pharmaceutical and life...

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Significant ROI from Doc Control System
QMS
Significant ROI from Doc Control System

Document Control Software System helps to increase your ROI ROI has always been...

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Strategic approach for Doc Control System
QMS
Strategic approach for Doc Control System

Where attendees learned about the best practices in the selection and...

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Motive switch to a Doc Control System from Paper
QMS
Motive switch to a Doc Control System from Paper

Where businesses become more important and job become hectic while manage all...

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Consequence of SOP and training records during audit
QMS
Consequence of SOP and training records during audit?

Introduction Ultimately, every person in a company is accountable for the...

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Sarjen System is a 25 years’ legacy brand holding rich experience with automation greenfield solutions with expertise in the Pharmaceutical and Life Science Industry. To begin your journey for digital transformation and automation, visit www.sarjen.com.

  • Recent Posts

    • How a TMS Solution in Pharma Improves Training Effectiveness and Audit Readiness
    • LMS in Pharmaceutical Industry: A Smarter Way to Manage Training and Audits
    • Best Practices for Training Management in Pharma: Ensuring Compliance and Skill Development
    • Why Every Pharma Company Needs a Learning Management System for Pharma training compliance
    • How a Training Management System in Pharmaceutical Industry Can Transform Workforce Compliance


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