Tag: FTA

How to Present Risk Analysis During Regulatory Inspections

How to Present Risk Analysis During Regulatory Inspections How to Present Risk Analysis During Regulatory Inspections Step 1: Understanding User Requirements Specification (URS) and Risk Assessment Before initiating any validation project, it is crucial to establish a comprehensive User Requirements…

Real-World Deviations Traced Back Through FTA Models

Real-World Deviations Traced Back Through FTA Models Real-World Deviations Traced Back Through FTA Models In the pharmaceutical industry, ensuring consistent quality of products is paramount. Understanding the complexities of validation processes, especially within the context of deviations, is critical. This…

Risk Tools for Cleaning Validation in Multi-Product Plants

Risk Tools for Cleaning Validation in Multi-Product Plants Risk Tools for Cleaning Validation in Multi-Product Plants The pharmaceutical industry is characterized by stringent regulatory requirements that emphasize the importance of product and process validation. For multi-product plants, the challenge is…

FMEA for Computer System Validation (CSV) Projects

FMEA for Computer System Validation (CSV) Projects FMEA for Computer System Validation (CSV) Projects: A Step-by-Step Guide Step 1: Understanding the URS and Risk Assessment Before embarking on any validation lifecycle, it is crucial to define clear User Requirements Specifications…

Common Mistakes in FMEA Risk Scoring and How to Fix Them

Common Mistakes in FMEA Risk Scoring and How to Fix Them Common Mistakes in FMEA Risk Scoring and How to Fix Them In the pharmaceutical industry, ensuring the quality and safety of products is paramount. This is where the product…

Linking Risk Assessment Outputs to Validation Protocols

Linking Risk Assessment Outputs to Validation Protocols Linking Risk Assessment Outputs to Validation Protocols Linking Risk Assessment Outputs to Validation Protocols – Practical guide for pharma professionals on iq oq and pq validation with GMP, FDA and EMA compliance. Step…

Writing SOPs for FMEA and HACCP in Pharma Facilities

Writing SOPs for FMEA and HACCP in Pharma Facilities Writing SOPs for FMEA and HACCP in Pharma Facilities This article provides a comprehensive step-by-step validation tutorial focusing on the essential aspects of SOP development for Failure Modes and Effects Analysis…

Risk Assessment Formats Accepted by FDA and EMA

Risk Assessment Formats Accepted by FDA and EMA Risk Assessment Formats Accepted by FDA and EMA Step 1: Understanding the Context of Risk Assessment in Validation Risk assessment is an essential component of the pharmaceutical validation lifecycle, particularly in relation…

Regulatory Expectations for Using Risk Tools in Validation

Regulatory Expectations for Using Risk Tools in Validation Regulatory Expectations for Using Risk Tools in Validation Validation in the pharmaceutical and biopharmaceutical industries is essential to ensure product quality, efficacy, and safety. A robust validation process adheres to established guidelines…

How to Apply FTA in Utility and HVAC Risk Scenarios

How to Apply FTA in Utility and HVAC Risk Scenarios How to Apply FTA in Utility and HVAC Risk Scenarios In the pharmaceutical industry, validating processes is a critical step to ensure quality and compliance with regulatory requirements. One essential…