Revalidation of Blister Machines After Change in Format

Revalidation of Blister Machines After Change in Format Revalidation of Blister Machines After Change in Format Revalidation of blister packaging machines is a critical process in ensuring the continued quality, safety, and efficacy of pharmaceutical products. With the continual evolution…

Air Permeability and Leak Rate Acceptance Criteria

Air Permeability and Leak Rate Acceptance Criteria Air Permeability and Leak Rate Acceptance Criteria Air permeability and leak rate acceptance criteria are crucial aspects of pharmaceutical packaging validation processes. Appropriate evaluations and qualifications ensure that the packaging systems effectively protect…

Common Blister Packaging Deviations and Their Root Causes

Common Blister Packaging Deviations and Their Root Causes Common Blister Packaging Deviations and Their Root Causes In the pharmaceutical industry, the validation of packaging systems is a critical component in ensuring product quality and regulatory compliance. Blister packaging, widely used…

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…

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…

Visual Inspection & Leak Test Parameters for Blister Packs

Visual Inspection & Leak Test Parameters for Blister Packs Visual Inspection & Leak Test Parameters for Blister Packs This detailed tutorial serves as a comprehensive guide for QA, QC, validation, and regulatory teams involved in the pharmaceutical validation of blister…

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…

Blister Packaging Validation: Sealing, Leak Testing, and PQ

Blister Packaging Validation: Sealing, Leak Testing, and PQ Blister Packaging Validation: Sealing, Leak Testing, and PQ In the pharmaceutical industry, packaging plays a crucial role in protecting product integrity, ensuring patient safety, and complying with regulatory standards. The validation of…

How to Document Packaging Configuration Changes in VMP

How to Document Packaging Configuration Changes in VMP How to Document Packaging Configuration Changes in VMP In the pharmaceutical industry, maintaining compliance with regulatory standards requires stringent processes and documentation practices. One crucial aspect of validation is managing changes to…

Dynamic Load Testing for Bulk Packaging Validation

Dynamic Load Testing for Bulk Packaging Validation Dynamic Load Testing for Bulk Packaging Validation In the pharmaceutical industry, robust validation processes are crucial to ensure product safety, quality, and compliance. This article provides a comprehensive step-by-step tutorial on dynamic load…