Tag: csv validation in pharma

Common Audit Findings Related to Transport and Storage Conditions

Common Audit Findings Related to Transport and Storage Conditions Common Audit Findings Related to Transport and Storage Conditions Step 1: Understanding User Requirements Specification (URS) & Risk Assessment The foundation of any effective validation process lies in a comprehensive User…

Accelerated vs Long-Term Stability Protocols Linked to Packaging

Accelerated vs Long-Term Stability Protocols Linked to Packaging Accelerated vs Long-Term Stability Protocols Linked to Packaging In the pharmaceutical industry, ensuring the long-term stability and integrity of products is paramount. Stability testing protocols, both accelerated and long-term, are critical components…

Common HVAC-Related Observations in 483s and Warning Letters

Common HVAC-Related Observations in 483s and Warning Letters Common HVAC-Related Observations in 483s and Warning Letters In the pharmaceutical industry, ensuring a validated and compliant HVAC system is critical for meeting regulatory standards and ensuring product quality. One of the…

Document Numbering and Naming Conventions for Validation

Document Numbering and Naming Conventions for Validation Document Numbering and Naming Conventions for Validation Document management is a critical component of the validation lifecycle in pharmaceuticals and medical devices. Particularly within the framework of CSV validation in pharma, adherence to…

Linking the VMP with Equipment, Cleaning, and CSV Plans

Linking the VMP with Equipment, Cleaning, and CSV Plans Linking the VMP with Equipment, Cleaning, and CSV Plans In the pharmaceutical and medical device industries, validation is essential to ensure compliance with regulations and to guarantee product quality and safety.…

Qualifying Cloud Vendors for Pharmaceutical Use

Qualifying Cloud Vendors for Pharmaceutical Use Qualifying Cloud Vendors for Pharmaceutical Use In the modern pharmaceutical landscape, the reliance on cloud-based systems is growing significantly. As organizations transition to these platforms for critical operations, ensuring compliance and validation aligns with…

Performing Gap Assessment for Qualification During Transfers

Performing Gap Assessment for Qualification During Transfers Performing Gap Assessment for Qualification During Transfers In the pharmaceutical industry, ensuring compliance with regulatory standards is paramount for product safety and efficacy. One critical component of this process is the validation of…

Why the Lifecycle Model Replaces One-Time Validation

Why the Lifecycle Model Replaces One-Time Validation Why the Lifecycle Model Replaces One-Time Validation The pharmaceutical industry is evolving, and so too must our approach to process validation. The traditional model, often based on a one-time validation exercise, is being…