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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
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  • Resources
    • Blogs
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    • 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

Document Management System (DMS) at a Glance
Document Management System
Document Management System (DMS) at a Glance

A Document Management System (DMS) is a system used to track, manage and...

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How 21 CFR Part 11 ensure data integrity in order to ensure product quality
21 CFR Part 11
How 21 CFR Part 11 ensure data integrity in order to ensure product quality?

Data Integrity is one of today’s hot topics in the Life Sciences industry The...

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How Technology has changed regulatory compliance in the Past Decade
21 CFR Part 11
How Technology has changed regulatory compliance in the Past Decade?

We live in a time of rapid change and information overload It helps to pause...

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Improve your quality benchmarks and raising credibility with Quality Management System
QMS
Improve your quality benchmarks and raising credibility with Quality Management System.

Quality management system refers to a set of processes, policies and procedures...

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The all about Computer System Validation in Pharmaceuticals
Computer System Validation
The all about Computer System Validation in Pharmaceuticals.

Computer system validation is the process of ensuring that any technology...

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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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