Installation Qualification , Good Manufacturing Practice

Recommendation on Validation Master Plan, Installation and Operational Qualification, Non-Sterile Process Validation and Cleaning Validation. This document is the basis for Annex 15 to the EC Guide on Good Manufacturing Practices for Medical Products. Figure 4 displays the most commonly used topics to be described in a VMP. 

Beyond the ROI issues, one of the premises for the use of advanced process analyzers is improved product quality. For many industries, and in particular industries close to consumers, there is the need to define procedures and installation qualification/oper-ational qualification/performance qualification (IQ/OQ/PQ) issues, good laboratory practice and good manufacturing practice (GLP/GMP), audit trails, etc. Such requirements open the door for the use of improved analytical methodology, which can be readily provided by the implementation of good process analyzer technology. 

Software and computer systems used in analytical laboratories that must comply with good laboratory practice (GLP) and good manufacturing practice (GMP) regulations require formal validation to confirm that they meet the criteria for intended use. Both new and existing systems, regardless of age, must be validated for their suitability for indented use. Whereas the first three articles in this series [1-3] focused on validation during development, vendor qualification, and installation and operational qualification of new systems, this article describes the procedures for systems that have been purchased, installed, and used prior to formal validation and that must be newly documented. 

EDMS = Electronic Document Management System MMS = Maintenance Management System BMS = Building Management System RCM reliability-centered maintenance SHE = Safety, Health and Environment OEM = Operation and Maintenance CMP = Good Manufacturing Practice IQ= Installation Qualification OQ = Operational Qualification... 

Samples applied with the ATS 4 can be positioned for normal, double-sided, or circular chromatographic development. Analyses performed with this applicator, combined with densitometric chromatogram evaluation controlled by the same PC with Windows-based WinCats software, comply with good manufacturing practices/ good lab practices (GMP/GLP), installation qualification (IQ)/operational qualification (OQ), and 21 Code of Federal Regulations (CFR) Part 11 (drug analysis) requirements. 

Computer hardware needs to be assembled in accordance with good practice and any manufacturer s instructions. Hardware components should be itemized in the Hardware Design and checked as part of the Installation Qualification. 

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