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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

Regulatory Expectations for Market Complaint Management in Pharma
Complaint management software
Regulatory Expectations for Market Complaint Management in Pharma

Regulatory Expectations for Market Complaint Management in Pharma  In...

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The Impact of Process Control on Reducing Out-of-Specification (OOS) Results
OOS & OOT management software
The Impact of Process Control on Reducing Out-of-Specification (OOS) Results

How Process Control Reduces OOS Results in Pharma Manufacturing  In...

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The Role of PQS in Ensuring Compliance with FDA Regulations
Pharmaceutical Quality System (PQS)
The Role of PQS in Ensuring Compliance with FDA Regulations

How PQS Ensures Compliance with FDA Regulations  Pharmaceutical manufacturers...

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Vendor Qualification Management Strategies
Vendor Qualification Management
Implementing Effective Vendor Qualification Management Strategies

In the pharmaceutical industry, the quality of the final product is...

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Schedule M Compliance
Complaint management software
Why Schedule M Compliance Is Crucial for Exporting to Regulated Markets

Pharmaceutical exports to regulated markets such as the US, EU, and Canada...

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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.

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