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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

What Is the True Cost of Not Having an eQMS
Enterprise quality management software
What Is the True Cost of Not Having an eQMS?

An electronic Quality Management System (eQMS) is a vital tool that helps...

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How you can overcome human errors in SOP management
SOP management software
How you can overcome human errors in SOP management

Standard Operating Procedures (SOPs) are crucial in the pharmaceutical industry...

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Enterprise Quality Management Software
Enterprise quality management software
What is Enterprise Quality Management Software (EQMS)?

EQMS, an Enterprise quality management software is emerging in the large...

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enterprise quality management software
Enterprise quality management software
5 Factors to consider before selecting an enterprise quality management software

Before exploring the factors for selecting enterprise quality management...

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Regulatory Audits
Audit Management Software
How to Prepare for a Pharmaceutical Regulatory Audits?

Quality A common word used by everyone to signify that the activity performed...

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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

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    • 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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