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PharmaWhiz Author January 1, 2020 Sitemap2020-01-01T07:09:48+00:00

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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
    • Management Review in Pharmaceutical Industry
    • 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

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    CAPA Corrective and Preventive actions critical consumable disinfectant validation Failure Investigation FDA warning letter Good Documentation Practices Good Manufacturing Practices Handling of regulatory inspection Human error MHRA GMP inspection n-plan p-sampling plan Pharmaceutical Process alarm Quality Oversight r-sampling plan raw material sampling Raw material supplier qualification Regulatory audit Regulatory inspection simulation study with swab Statistical Evaluation of MHRA GMP inspection deficiencies year 2018 Subject matter expert Supplier supplier qualification Technology transfer of product unidirectional air flow URS User Requirement Specification for equipment
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