Tag: iso 1 clean room

Presenting KPI Dashboards to Regulatory Agencies

Presenting KPI Dashboards to Regulatory Agencies Presenting KPI Dashboards to Regulatory Agencies In the highly regulated pharmaceutical industry, presenting Key Performance Indicator (KPI) dashboards effectively to regulatory agencies is crucial for compliance and operational excellence. This article will provide a…

Digital CPV Templates for Process Owners and QA

Digital CPV Templates for Process Owners and QA Digital CPV Templates for Process Owners and QA The pharmaceutical industry is governed by strict regulatory standards to ensure the safety and efficacy of products. Among these, continued process verification (CPV) plays…

Gowning Room Qualification for Personnel Entry

Gowning Room Qualification for Personnel Entry Gowning Room Qualification for Personnel Entry In the pharmaceutical industry, maintaining a controlled environment for aseptic processes is paramount to ensure product quality and patient safety. Gowning rooms are critical components of this controlled…

Regulatory Requirements for Validation vs Revalidation Terminology

Regulatory Requirements for Validation vs Revalidation Terminology Regulatory Requirements for Validation vs Revalidation Terminology The pharmaceutical industry operates under stringent regulations to ensure the quality and safety of products. Central to these regulations is the validation lifecycle, which encompasses various…

Documenting Risk Identification in ICH Q9 Framework

Documenting Risk Identification in ICH Q9 Framework Documenting Risk Identification in ICH Q9 Framework This article provides a comprehensive step-by-step tutorial on validating the requirements set forth by the ICH Q9 guideline, specifically focusing on risk management within the pharmaceutical…

SST Failures: Root Cause Analysis and CAPA Approach

SST Failures: Root Cause Analysis and CAPA Approach SST Failures: Root Cause Analysis and CAPA Approach In the highly regulated pharmaceutical industry, validation processes are pivotal to ensuring product quality and compliance with established standards. This comprehensive guide outlines a…

Writing a Clean Steam Validation Protocol

Writing a Clean Steam Validation Protocol Writing a Clean Steam Validation Protocol In the pharmaceutical and biotechnology industries, maintaining sterile conditions is critical. This is particularly true for facilities utilizing clean steam systems, especially those operating under ISO 1 clean…

In-Process Control for Blend Uniformity in Granulation

In-Process Control for Blend Uniformity in Granulation In-Process Control for Blend Uniformity in Granulation In the pharmaceutical manufacturing process, ensuring blend uniformity is critical to product quality and efficacy. This article provides a comprehensive step-by-step validation tutorial focused on in-process…