Tag: validation in pharma company

How to Validate Placement of Sensors Inside Shipping Units

How to Validate Placement of Sensors Inside Shipping Units How to Validate Placement of Sensors Inside Shipping Units In the pharmaceutical industry, ensuring the integrity of products throughout the entire supply chain is paramount. This is particularly true regarding temperature-sensitive…

Distribution Qualification Studies Linked to Packaging Systems

Distribution Qualification Studies Linked to Packaging Systems Distribution Qualification Studies Linked to Packaging Systems In the pharmaceutical industry, rigorous validation processes are mandatory for ensuring the efficacy and safety of drug products during distribution. This article will guide QA, QC,…

Real-Time Monitoring of Package Conditions During Transit

Real-Time Monitoring of Package Conditions During Transit Real-Time Monitoring of Package Conditions During Transit In the pharmaceutical industry, ensuring the integrity of products during transit is crucial. This article provides a comprehensive, step-by-step guide on the validation in a pharma…

Heat Seal Temperature Mapping in Blister Machine Qualification

Heat Seal Temperature Mapping in Blister Machine Qualification Heat Seal Temperature Mapping in Blister Machine Qualification In the pharmaceutical industry, the validation of packaging processes is critical to ensuring product quality, compliance, and patient safety. This article will provide a…

Validation of Blister Cartoning Equipment: PQ Parameters

Validation of Blister Cartoning Equipment: PQ Parameters Validation of Blister Cartoning Equipment: PQ Parameters Validation in a pharmaceutical company is a critical process that ensures the quality, safety, and efficacy of pharmaceutical products. This article will provide a comprehensive, step-by-step…

Common Packaging Damage Points in Distribution and Their Mitigation

Common Packaging Damage Points in Distribution and Their Mitigation Common Packaging Damage Points in Distribution and Their Mitigation In the pharmaceutical sector, ensuring the integrity and functionality of packaging is not just a regulatory requirement but a critical component of…

Real-Time Monitoring of Cleanroom HVAC Performance

Real-Time Monitoring of Cleanroom HVAC Performance Real-Time Monitoring of Cleanroom HVAC Performance In the pharmaceutical and biologics sectors, maintaining a controlled environment is pivotal for product quality and compliance. This article outlines a clear, step-by-step validation lifecycle focused on cleanroom…

Writing a Combined HVAC Qualification Report: IQ/OQ/PQ in One

Writing a Combined HVAC Qualification Report: IQ/OQ/PQ in One Writing a Combined HVAC Qualification Report: IQ/OQ/PQ in One In the constantly evolving pharmaceutical landscape, ensuring the integrity of the HVAC (Heating, Ventilation, and Air Conditioning) systems is paramount for compliance…

Testing Differential Pressure, Velocity, and Clean-Up Time

Testing Differential Pressure, Velocity, and Clean-Up Time Testing Differential Pressure, Velocity, and Clean-Up Time The validation in pharma company is essential to ensure compliance with regulatory requirements while maintaining product quality and patient safety. This article provides a step-by-step tutorial…

Linking Risk Assessments to Validation Documentation

Linking Risk Assessments to Validation Documentation Linking Risk Assessments to Validation Documentation In the pharmaceutical industry, ensuring the safety and efficacy of products through effective validation processes is paramount. The integration of risk assessments into validation documentation not only enhances…