At IPP, we fully recognize the rigorous compliance requirements of Cleanroom Industries. Our design-build approach streamlines the design phase and reduces on-site labor, ensuring greater efficiency. By leveraging our expertise alongside a top engineering team, we deliver the design-build benefits that our clients need to create world-class facilities.
Our deep understanding of GMP (Good Manufacturing Practice) allows us to evaluate projects comprehensively, optimize planning, and anticipate operational issues. This approach ensures a seamless execution of the work, adhering to both current National and International standards.
A critical component of any cleanroom facility is the HVAC system, which must be designed and implemented in strict compliance with international standards. With extensive experience from over 20 global projects, IPP excels in setting up optimized HVAC systems that meet all relevant guidelines.
We handle HVAC projects from Concept to Commissioning, covering all aspects including URS (User Requirement Specification), System Design, Procurement of both high and low-side components, Installation, Testing & Commissioning, and Validation.
At IPP, we analyze your specific requirements to design and select the ideal HVAC system for your facility, ensuring optimal performance and compliance.
The standards of good manufacturing practice (cGMP) require special attention to risk assessment and verification procedures: “it is requirement of good manufacturing identify the activities of validation necessary to demonstrate control critical aspects of particular operations. The significant changes made to installations, equipment and processes, which may affect product quality, should be validated. A procedure for risk assessment should be used to determine the scope and extent of validation.”
The Validation Master Plan serves to make sure that all equipment, procedures, that may affect the quality or integrity or effectiveness of the product, are validated; it contains the general principles which comply during the validation task, and plans activities to be carried out for this purpose.
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