Tag: Qualification of Vendors & Materials

Packaging Component Change Control and Requalification

Packaging Component Change Control and Requalification Packaging Component Change Control and Requalification This article serves as a comprehensive step-by-step tutorial on the packaging component change control and requalification process. It is tailored for pharmaceutical professionals engaged in iopq validation, ensuring…

Regulatory Guidelines for Container-Closure System Qualification

Regulatory Guidelines for Container-Closure System Qualification Regulatory Guidelines for Container-Closure System Qualification In the pharmaceutical industry, ensuring the integrity and safety of drug products is paramount. A critical aspect of this process is the qualification of container-closure systems (CCS). This…

Testing Requirements for Blister Foil, Bottles, and Stoppers

Testing Requirements for Blister Foil, Bottles, and Stoppers Testing Requirements for Blister Foil, Bottles, and Stoppers The pharmaceutical industry must adhere to stringent regulatory frameworks to ensure the safety and efficacy of its products. One critical component of this framework…

Label Qualification: Print Durability, Adhesive, and Regulatory Info

Label Qualification: Print Durability, Adhesive, and Regulatory Info Label Qualification: Print Durability, Adhesive, and Regulatory Info In the highly regulated pharmaceutical and biologics industry, ensuring the integrity of labels used on packaging is paramount. Label qualification encompasses various aspects, including…

Dimensional, Visual, and Functional Testing of Packaging Components

Dimensional, Visual, and Functional Testing of Packaging Components Dimensional, Visual, and Functional Testing of Packaging Components Packaging plays a critical role in the pharmaceutical industry. The integrity, safety, and effectiveness of pharmaceutical products depend largely on the quality of their…

Migration and Compatibility Studies in Packaging Material Qualification

Migration and Compatibility Studies in Packaging Material Qualification Migration and Compatibility Studies in Packaging Material Qualification In the pharmaceutical industry, ensuring the integrity and safety of products during storage and transit is crucial. Packaging materials play a vital role in…

How to Qualify Packaging Vendors in GMP Facilities

How to Qualify Packaging Vendors in GMP Facilities How to Qualify Packaging Vendors in GMP Facilities Qualifying packaging vendors in the pharmaceutical industry is a critical component of ensuring that packaged products meet the required quality standards and comply with…

Primary vs Secondary Packaging Qualification Requirements

Primary vs Secondary Packaging Qualification Requirements Primary vs Secondary Packaging Qualification Requirements 1. Understanding User Requirements Specification (URS) and Risk Assessment In the pharmaceutical industry, the validation process revolves around an essential first step: creating a User Requirements Specification (URS).…

Requalifying Materials After Supplier Change or Route Modification

Requalifying Materials After Supplier Change or Route Modification Requalifying Materials After Supplier Change or Route Modification In the highly regulated pharmaceutical industry, requalifying materials after a supplier change or modification of the manufacturing route is a fundamental process that ensures…

Case Study: Raw Material Qualification Deficiency in FDA 483

Case Study: Raw Material Qualification Deficiency in FDA 483 Case Study: Raw Material Qualification Deficiency in FDA 483 This article provides an in-depth exploration of the raw material qualification process, particularly in the context of compliance with FDA regulations. It…