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• Category: Equipment Qualification & Validation
  • How to prepare User Requirement Specification
• Category: Good Automated Manufacturing Practices
  • Process alarm and Its significance during pharmaceutical product manufacturing
  • Electronic Batch Record in Pharmaceutical and Its benefits
• Category: Good Documentation Practices
  • How to implement Good Documentation Practices
• Category: Good Laboratory Practices
  • HPLC Troubleshooting & Its Data Integrity Assessment
• Category: Good Manufacturing Practices
  • Trend Analysis a tools for Risk-Based thinking
  • 5 ways to reduce Human Error
  • Quality Oversight – an USFDA warning letter
  • Media fill aseptic processing
  • Handling of consumables in pharmaceutical industries
  • SOP on Technology Transfer
  • Microbial Contamination in Pharmaceutical products
  • Raw Material Supplier Selection And Qualification in Pharmaceutical
  • Sampling of Raw Material used in the Pharmaceutical Drug Product Preparation
  • Category: Audit & Compliance
    • Statistical Analysis of MHRA 2018 GMP Inspection’s Deficiencies
• Category: Others
  • COVID-19 (Corona Virus) and Unethical Business
• Category: QMS
  • Risk Management Approach
  • Common Mistakes during Investigation of failure
• Category: Standard Operating Procedure
  • SOP on handling of Regulatory Audit
• Category: Validation
  • Disinfectant validation and its significance in pharmaceutical industries