Tag: Sterility Assurance & Contamination Control

Equipment Disinfection vs Sterilization: What’s Required Where?

Equipment Disinfection vs Sterilization: What’s Required Where? Equipment Disinfection vs Sterilization: What’s Required Where? The assurance of sterility in pharmaceutical environments is critical, particularly in maintaining product integrity and patient safety. With the evolving landscape of regulations and technologies, understanding…

Using Risk Assessment for Contamination Control Justification

Using Risk Assessment for Contamination Control Justification Using Risk Assessment for Contamination Control Justification Cleaning validation is a cornerstone of contamination control in the pharmaceutical industry. This guide offers a comprehensive overview of the validation lifecycle for cleaning processes through…

Visual Inspection as Part of Sterility Assurance Strategy

Visual Inspection as Part of Sterility Assurance Strategy Visual Inspection as Part of Sterility Assurance Strategy In the pharmaceutical industry, the integrity and sterility of products are paramount for patient safety. Among various methodologies, visual inspection plays a critical role…

How to Build a Sterility Assurance Program in Pharma

How to Build a Sterility Assurance Program in Pharma How to Build a Sterility Assurance Program in Pharma In the pharmaceutical industry, a Sterility Assurance Program (SAP) is essential for ensuring that products meant for human use are free from…

Establishing Contamination Control Strategies for Grade A/B Areas

Establishing Contamination Control Strategies for Grade A/B Areas Establishing Contamination Control Strategies for Grade A/B Areas The pharmaceutical industry heavily relies on stringent contamination control measures in Grade A/B areas to ensure the sterility and quality of products. This tutorial…

Sterility Assurance Level (SAL) in Aseptic Processing Explained

Sterility Assurance Level (SAL) in Aseptic Processing Explained Sterility Assurance Level (SAL) in Aseptic Processing Explained In pharmaceutical manufacturing, particularly within aseptic processing, achieving an acceptable Sterility Assurance Level (SAL) is critical to ensure product safety and efficacy. The principles…