Tag: packaging material qualification

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).…

Ensuring Container/Closure Compatibility & Safety

Ensuring Container/Closure Compatibility & Safety How to Ensure Container and Closure Compatibility and Safety in Pharma Packaging Pharmaceutical packaging does more than contain the drug—it protects its stability, potency, and safety throughout its shelf life. Container and closure systems must…