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Welcome to Pharmaceutical Blog

Here you can read Pharmaceuticals Standard Operating Procedures (SOP), Guidelines,
Method of Analysis, Test Procedures, Instruments Calibrations and Validation.
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PharmaBlog
PharmaBlog

Welcome to Pharmaceutical Blog

  • About
  • Contact us
  • Copyright Policy and Terms of Use
  • Disclaimer
  • Guidelines
  • Method of Analysis (MOA)
  • Microbiology
  • Packaging Materials
  • Privacy Policy
  • Quality Assurance
  • Quality Control
  • Sitemap
  • Validation

SOP vs STP

pharmablog.in / Guidelines / November 4, 2025 / guideline / Leave a Comment

Learn the difference between SOP (Standard Operating Procedure) and STP (Standard Testing Procedure) in pharmaceuticals — their purpose, scope, and importance in GMP compliance.

SOP vs STP Read More »

Swab Sampling in Pharmaceuticals

pharmablog.in / Guidelines / November 4, 2025 / guideline / Leave a Comment

Swab sampling is a key GMP practice for verifying equipment cleanliness and preventing cross-contamination. Learn its purpose, procedure, and role in pharmaceutical quality assurance.

Swab Sampling in Pharmaceuticals Read More »

LOD vs Moisture Content

pharmablog.in / Guidelines / November 4, 2025 / guideline / Leave a Comment

earn the key differences between LOD (Loss on Drying) and Moisture Analyzer methods. Understand their principles, purpose, and applications in pharmaceutical, food, and chemical industries.

LOD vs Moisture Content Read More »

Deviation vs Incident

pharmablog.in / Guidelines / November 4, 2025 / guideline / Leave a Comment

Learn the key difference between a deviation and an incident in pharmaceutical manufacturing. Understand how each is managed under GMP and PQS, with examples and guideline references.

Deviation vs Incident Read More »

The Basics of Quality Management Systems (QMS)

pharmablog.in / Guidelines / November 4, 2025 / guideline / Leave a Comment

Discover the fundamentals of a Quality Management System (QMS) — its principles, benefits, types, and real-world applications across industries. Learn how QMS drives efficiency, compliance, and customer satisfaction.

The Basics of Quality Management Systems (QMS) Read More »

💊 Pharmaceutical Document Control – GMP Essentials

pharmablog.in / Guidelines / November 4, 2025 / guideline / Leave a Comment

Learn the essentials of Pharmaceutical Document Control as per GMP guidelines. Understand ALCOA+ data integrity principles, document lifecycle, retention, and destruction procedures with practical examples.

💊 Pharmaceutical Document Control – GMP Essentials Read More »

What Is Quality Control TAT? Meaning, Importance & How to Improve It

pharmablog.in / Guidelines / November 4, 2025 / Leave a Comment

Learn what Quality Control Turnaround Time (QC TAT) means, why it’s important, and how to calculate and improve it in manufacturing or laboratory environments. Simple guide with examples.

What Is Quality Control TAT? Meaning, Importance & How to Improve It Read More »

Quality Control Department Incidents – HPLC Instrument Malfunction

pharmablog.in / Incident / August 29, 2025 / incident

Incident Report Format |  Incident Report Template | Incident Report Format For Quality Control Department Incidents | Incident Report HPLC Instrument Malfunction |   

Quality Control Department Incidents – HPLC Instrument Malfunction Read More »

Regulatory & Compliance Incidents-Non-compliance observed during self-inspection or regulatory audits

pharmablog.in / Incident / August 29, 2025 / incident

Incident Report Format |  Incident Report Template | Incident Report Format For Regulatory & Compliance Incidents | Incident Report For Non-compliance observed during self-inspection or regulatory audits |   

Regulatory & Compliance Incidents-Non-compliance observed during self-inspection or regulatory audits Read More »

Warehouse & Logistics Incidents-Wrong material issuance (mix-up in API/excipient/packing material)

pharmablog.in / Incident / August 29, 2025 / incident

Incident Report Format |  Incident Report Template | Incident Report Format For Warehouse & Logistics Incidents | Incident Report For Wrong material issuance (mix-up in API/excipient/packing material) |   

Warehouse & Logistics Incidents-Wrong material issuance (mix-up in API/excipient/packing material) Read More »

1 2 … 22 Next →
  • Guidelines
  • Incident
  • Method of Analysis
  • Microbiology
  • Packaging Material
  • Quality Assurance
  • Quality control
  • SOP
  • Validation
  • SOP vs STP
  • Swab Sampling in Pharmaceuticals
  • LOD vs Moisture Content
  • Deviation vs Incident
  • The Basics of Quality Management Systems (QMS)

Mr. Shaikh is the professional pharmaceuticals blogger, founder and author of PharmaBlog.in

  • SOP vs STP
  • Swab Sampling in Pharmaceuticals
  • LOD vs Moisture Content
  • Deviation vs Incident
  • The Basics of Quality Management Systems (QMS)
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