Tag: validation in pharmaceutical industry

SOP for Retrieving and Interpreting Logger Data Post Shipment

SOP for Retrieving and Interpreting Logger Data Post Shipment SOP for Retrieving and Interpreting Logger Data Post Shipment This article serves as a comprehensive step-by-step tutorial for retrieving and interpreting logger data post shipment within the validation in pharmaceutical industry.…

Calibration and Accuracy Verification of Monitoring Devices

Calibration and Accuracy Verification of Monitoring Devices Calibration and Accuracy Verification of Monitoring Devices Calibration and accuracy verification of monitoring devices are critical components of validation in the pharmaceutical industry. These activities ensure that instruments used in monitoring conditions during…

Case Study: Validation Failure Due to Inadequate Packaging

Case Study: Validation Failure Due to Inadequate Packaging Case Study: Validation Failure Due to Inadequate Packaging This article aims to provide pharmaceutical professionals a methodical approach to understanding the validation lifecycle—specifically focusing on the failure due to inadequate packaging. By…

How to Validate Pocket Integrity in Cold-Form Foil Blisters

How to Validate Pocket Integrity in Cold-Form Foil Blisters How to Validate Pocket Integrity in Cold-Form Foil Blisters Validation in the pharmaceutical industry is a critical requirement for ensuring that products meet their specifications and quality criteria. This article provides…

Strip Packing Machine Qualification: From Foil Feed to Final Pack

Strip Packing Machine Qualification: From Foil Feed to Final Pack Strip Packing Machine Qualification: From Foil Feed to Final Pack In the pharmaceutical industry, ensuring that packaging processes meet regulatory standards is crucial for product safety and efficacy. Validation in…

Qualification of Outer Packaging Lines for Labeling & Coding

Qualification of Outer Packaging Lines for Labeling & Coding Qualification of Outer Packaging Lines for Labeling & Coding The pharmaceutical industry operates under strict regulations to ensure that products are manufactured, tested, and delivered in a manner that guarantees quality…

Airborne Microbial Monitoring: Settle Plates vs Active Air Sampling

Airborne Microbial Monitoring: Settle Plates vs Active Air Sampling Airborne Microbial Monitoring: Settle Plates vs Active Air Sampling Ensuring the quality and safety of pharmaceutical products requires stringent environmental monitoring practices, particularly in areas where airborne microbial contamination can occur.…

How to Perform Filter Integrity (Leak) Tests for PQ

How to Perform Filter Integrity (Leak) Tests for PQ How to Perform Filter Integrity (Leak) Tests for PQ In the pharmaceutical industry, maintaining product quality and ensuring compliance with regulatory standards is critical. Filter integrity testing is an essential aspect…

Best Practices for Traceability in Lifecycle Validation

Best Practices for Traceability in Lifecycle Validation Best Practices for Traceability in Lifecycle Validation In the pharmaceutical industry, validation is a crucial process that ensures products are consistently manufactured to the required quality standards. This comprehensive guide focuses on best…