Tag: and Label Validation

Manual vs Automated Labeling: Validation Challenges and Tips

Manual vs Automated Labeling: Validation Challenges and Tips Manual vs Automated Labeling: Validation Challenges and Tips In the pharmaceutical industry, ensuring the integrity and reliability of labeling systems is critical for compliance with regulatory standards and maintaining product quality. This…

Integration of ERP and Serialization Systems in Validation

Integration of ERP and Serialization Systems in Validation Integration of ERP and Serialization Systems in Validation In the pharmaceutical industry, validation is a critical aspect of ensuring compliance with regulatory requirements and maintaining product integrity. This article serves as a…

Coding Equipment Qualification: IQ/OQ/PQ Protocols

Coding Equipment Qualification: IQ/OQ/PQ Protocols Coding Equipment Qualification: IQ/OQ/PQ Protocols In the pharmaceutical and biologics sectors, ensuring that coding equipment operates within defined specifications is critical for compliance with Good Manufacturing Practices (GMP) and other regulatory frameworks. This comprehensive guide…

Label Stock Qualification: Adhesive Strength, Print Durability

Label Stock Qualification: Adhesive Strength, Print Durability Label Stock Qualification: Adhesive Strength, Print Durability In the pharmaceutical industry, ensuring the integrity and compliance of packaging systems is paramount. One critical aspect of this process is the qualification of label stock,…

Print Quality Validation for 2D Codes, Datamatrix & Barcodes

Print Quality Validation for 2D Codes, Datamatrix & Barcodes Print Quality Validation for 2D Codes, Datamatrix & Barcodes In today’s pharmaceutical landscape, ensuring product integrity through effective print quality validation for 2D codes, DataMatrix, and barcodes is essential. This article…

How to Validate a Serialization System: Pharma Industry Guide

How to Validate a Serialization System: Pharma Industry Guide How to Validate a Serialization System: Pharma Industry Guide Step 1: Understanding User Requirements Specification (URS) and Risk Assessment The first phase in the validation lifecycle for a serialization system begins…