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Read more about the article Selecting Surfaces for Disinfectant Efficacy Testing in the Pharmaceutical Industry
Aseptic Manufacturing / Microbiology

Selecting Surfaces for Disinfectant Efficacy Testing in the Pharmaceutical Industry

Disinfectant efficacy testing is one of the most critical components in the pharmaceutical industry, particularly the surface…

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February 12, 2026
Read more about the article How to Handle Out-of-Specification (OOS) Results in QC Testing
Quality Assurance / Quality Control

How to Handle Out-of-Specification (OOS) Results in QC Testing

Finding the out-of-Specification (OOS) results is one of the most stressful moments in a pharmaceutical quality control…

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February 10, 2026
Read more about the article Fluid Thioglycollate Medium (FTM) in Sterility Testing
Microbiology

Fluid Thioglycollate Medium (FTM) in Sterility Testing

Sterility testing is one of the most sensitive microbiological tests performed in the pharmaceutical industry, and Fluid…

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February 8, 2026
Read more about the article Sterility Assurance and Sterility Assurance Level (SAL) in Pharmaceutical Products
Quality Assurance / Sterility Assurance / Validation and Qualification

Sterility Assurance and Sterility Assurance Level (SAL) in Pharmaceutical Products

Sterile pharmaceutical products demand more than just a successful sterilization cycle. They require a holistic system of…

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February 4, 2026
Read more about the article Parametric Release in Pharmaceuticals
Quality Assurance / Validation and Qualification

Parametric Release in Pharmaceuticals

In pharmaceutical manufacturing, product release traditionally depends on finished product testing, especially sterility testing. However, for certain…

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February 4, 2026
Read more about the article Real-World Documentation Errors in Pharma: Lessons from the Shop Floor
Audits and Compliance / Documentation / GMP

Real-World Documentation Errors in Pharma: Lessons from the Shop Floor

Documentation errors in pharma are the most common reasons for audit observations. These errors may occur even…

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February 2, 2026

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Recent Posts

  • Selecting Surfaces for Disinfectant Efficacy Testing in the Pharmaceutical Industry
    Selecting Surfaces for Disinfectant Efficacy Testing in the Pharmaceutical Industry
    February 12, 2026/
    0 Comments
  • How to Handle Out-of-Specification (OOS) Results in QC Testing
    How to Handle Out-of-Specification (OOS) Results in QC Testing
    February 10, 2026/
    0 Comments
  • Fluid Thioglycollate Medium (FTM) in Sterility Testing
    Fluid Thioglycollate Medium (FTM) in Sterility Testing
    February 8, 2026/
    0 Comments
  • Sterility Assurance and Sterility Assurance Level (SAL) in Pharmaceutical Products
    Sterility Assurance and Sterility Assurance Level (SAL) in Pharmaceutical Products
    February 4, 2026/
    0 Comments
  • Parametric Release in Pharmaceuticals
    Parametric Release in Pharmaceuticals
    February 4, 2026/
    0 Comments
  • Real-World Documentation Errors in Pharma: Lessons from the Shop Floor
    Real-World Documentation Errors in Pharma: Lessons from the Shop Floor
    February 2, 2026/
    0 Comments
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