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WELCOME TO VENAIR SOLUTIONS
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Who We Are
At Venair Solutions, we are industry leaders in clean room validation and services, dedicated to ensuring your controlled environments meet the highest standards of quality, compliance, and efficiency. With a team of experienced professionals, we specialize in comprehensive clean room certification, performance testing, and maintenance tailored to diverse industries such as pharmaceuticals, biotechnology, healthcare, and electronics. Our mission is to deliver reliable solutions that optimize clean room performance, safeguard product integrity, and exceed regulatory requirements. Trust us to be your partner in creating environments that foster innovation and operational excellence.
Our Services
HVAC and Clean Room
We specialize in delivering advanced HVAC and clean room solutions tailored to meet the highest industry standards. Our HVAC systems ensure precise temperature, humidity, and air quality control for optimal comfort and energy efficiency in residential, commercial, and industrial spaces. For industries requiring ultra-clean environments, such as pharmaceuticals, healthcare, and electronics, our clean room solutions are engineered to maintain stringent air purity, particulate control, and contamination-free conditions. With cutting-edge technology and expert craftsmanship, we provide customized designs and installations that guarantee reliability, compliance, and performance excellence.
Heating, ventilation, and air conditioning - HVAC s the technology of indoor and vehicular environmental comfort. It's goal is to provide thermal comfort and acceptable indoor air quality. HAVC and Pharmaceutical Clean rooms require strict environmental controls to ensure the manufacture of quality products. controls regulate a wide range of Conditions such as airborne Particulate , Temperature, Humidiy.
On Site HVAC Validation
- Air Velocity ACPH Test
- Filter Integrity Test
- Temp/Humidity Test
- Luminous Test
- Particle Count Test
- Sound Level Test
- Particle Recovery Test
- Differential Pressure Test
- Air Flow Pattern Test
Flow Units
When you require a clean environment workstation, Pro Cleanroom offers a solution with its laminar flow units. Through unidirectional airflow, a particle free environment is created that allows critical process to run according to the highest standards.The air in the LAF unit is free from particles and micro-organisms and protects against harmful product and process contamination.
What is unidirectional airflow?
Unidirectional airflow represents an air flow in one direction without interruption by turbulence. In a LAF units, the air flows in a unidirectional pattern from the HEPA or ULPA filter surface. This may be a horizontal Flow (crossflow) or a vertical flow (downflow).
Commissioing and Qualification of Projects
Basic Design
- Development of user requirement specification For the Procees equipments
- Vendor evaluation and Finalization [Technical]
Detail Design Phase /Pre-Commissioning Phase
- Development of Validation strategy based on the client requirement
- Development of Validation master plan
- Development of Project SOPs, Templates for C&Q
- Development of C and Q plan for Clean utility
- Development of C and Q plan for Black utility
Commissioning and Qualification phase
- Risk assessment preparation
- URS finalization
- Vendor DQ reviews and finalization
- Requirement tracebility matrix preparation
- FAT protocol review
We Serve Wide-range of Supported Industries
Pharmaceutical & Healthcare
Aerospace & Defence
Automotive
Electrical & Electronics
Food Processing
Semiconductor Production
How We Work
FOR SMART & SAFER SOLUTION !!
Why Choose Us
Product Safety
Clean room validation ensures that the quality of your products remains uncompromised by verifying the cleanliness of the environment where they are manufactured, packaged, or stored. This minimizes the risk of contamination-related defects and protects your brand reputation.
Regulatory Compliance
Regulatory bodies, such as the FDA, MHRA, and EMA, mandate clean room validation for industries like pharmaceuticals, medical devices, and biotechnology. By adhering to these regulations, you demonstrate your commitment to safety, efficacy, and compliance.
Operational Efficiency
Clean room validation identifies areas of improvement within your facility, allowing you to optimize your processes and minimize operational disruptions. By addressing potential issues proactively, you can enhance productivity, reduce downtime, and maximize resource utilization.
Employee Safety
Clean rooms often handle hazardous materials, and maintaining a safe working environment is crucial for your employees. Regular validation provides assurance that appropriate control measures are in place to protect personnel from airborne contaminants and other occupational hazards.
Our Client Base
ABOUT US
We are industry leaders in clean room validation and services, dedicated to ensuring your controlled environments meet the highest standards of quality, compliance, and efficiency.
No-25, Sri Sumukha Nivas, APC Circle, Jigani Industrial Area, Anekal(Taluk), Bangalore - 560105.
+91 7204847026 +91 7204847028 +91 9591771170
services@venairsolutions.comnandish@venairsolutions.cominfo@venairsolutions.com
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