HVAC & Air Handling Systems

HVAC & Air Handling Systems

HVAC & Air Handling Systems

Deliberty Technicals designs critical environments and builds cleanrooms to ISO 14644 1, 2, 3 Requirements. For Life Sciences cleanrooms such as pharmaceutical from Manufacturing Suites, Packaging to sterile & aseptic fill suites, Neutraceuticals production, medical devices, biotechnology, ophthalmic, and biological safety laboratories.
Our projects have been validated to meet cGMP, FDA, EU standards. We can provide DQ, IQ & OQ documentation and execution and assist with PQ and SOP’s.

Our custom manufacturing of the air handling systems for critical environments gives us the advantage of understanding one of the most important aspects of the Cleanroom, the close tolerance control of temperature, humidity, air changes, and clean room pressures to provide cascading pressure differentials.

Our Mission is to enhance the knowledge and skills of the project team for the successful delivery of specialty environments with our systems expertise.

Building Management Systems


We Manufacture Air Handling Systems for Critical Environments to control Temperature, Humidity & Pressure for Cleanrooms, Biological Safety Containment, and Laboratories.

Our flexible modular design allows us to customize the size and layout of the system components to meet the individual requirements of your Critical Environment.

We utilize custom components selected for the individual system requirements, to maintain the required conditions.

Our HVAC Division Caters


Deliberty Controls offers specialized, high quality, integrated building management solutions by providing innovative design solutions, cost effective high quality instruments with excellent commissioning.
Our key to success is our management who bring along with them over two decades of experience in various field of industry. Proof of smart hard work is the receiving of the prestigious appreciation with a proven track record of successful project execution & final handover in our industry.
Deliberty Controls core strength is our capability to work with various building automation systems & its integration with other automaton system to give customers a comprehensive value-based solutions to enrich & maintain their system. Our knowledge for FDA CFR compliance and validation support services enhances our support to the Pharmaceutical industry.
Title 21 CFR Part 11 of the Code of Federal Regulations deals with the Food and Drug Administration (FDA) guidelines on electronic records and electronic signatures in the United States. Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).
There are many systems available to provide a the 21 CFR Part 11 hardware and Software, many which come with prepared IQ / OQ Documentation.
Utilizing the approach to simplify the validated critical system components to only the required inputs simplifies the entire process.

HVAC and Air handling systems;

Cleanroom Equipment