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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

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...

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Vendor-qualification
QMS
Vendor qualification

All pharmaceutical drugs are dealing with lives of patients Slightest of...

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5 Whys Investigation
QMS
5 Whys Investigation

QMS is an incident quality investigation tool used for investigating the root...

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Importance of Document Issuance
Document Issuance
Importance of Document Issuance

Document Issuance is a set procedure used to issue documents inside and outside...

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Control over Use of Superseded Document
Document Control
Control over Use of Superseded Document

In pharmaceutical and regulated industries, lots of changes are made in 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

    • Digital QMS and PQR: Top Integration Questions Answered
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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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