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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

QMS
The Critical Role of Vendor Qualification in Pharma Manufacturing

Why Vendor Qualification in Pharma is Essential  In your pharmaceutical...

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Quality Management 
Tackling Deviation Challenges in Pharma: Why Proactive Management is Essential

In pharmaceutical manufacturing, deviations are not just an...

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Audit Management Software
Are You Truly Prepared for Your Next Pharmaceutical Regulatory Audit?

In the pharmaceutical industry, regulatory audits are non-negotiable, essential...

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PQR
Quality Management 
Ensuring Compliance and Quality with Product Quality Reviews (PQR)

In the highly regulated pharmaceutical industry, maintaining product quality...

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Change Control
QMS
Gain Full Control Over Your Pharmaceutical Processes with Effective Change Control

Change Control in Pharmaceutical Manufacturing: Why It’s Critical  Yes,...

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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

    • Digital QMS and PQR: Top Integration Questions Answered
    • Regulatory Inspectors and PQR: Questions They Commonly Ask
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    • Multi-Region Compliance: Aligning PQR Practices Across Global Regulatory Bodies
    • Involving the Shop Floor in the PQR Process: A Bottom-Up Approach


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