Clean Room Validation Service

We provide and extensive range of services pertaining tyo Clean Room Validation by our panel of expert professionals available with us. Our service range includes, DOP/PAO HEPA Filter Integrity Test, Air velocity measurement, particle count test, room pressurization test, air flow visualization test, temperature and humidity, light intensity etc.  

Saakvee Technologies lead the way in designing and installing a wide range of customised cleanrooms, including modular cleanrooms, monobloc cleanrooms, hardwall cleanrooms, and softwall cleanrooms that meet the highest international installation and validation qualification standards across various industries. ISO 14644 is just one of the installation and cleanroom validation testing qualifications Saakvee Technologies adhere to.   Testing And Validation Cleanroom validation and testing ensures a totally secure environment and ISO compliance. It provides peace of mind that your cleanroom is performing according to specification and that Saakvee are looking after your cleanroom compliance.   Saakvee Technologies testing and validation is performed by CTCB-i trained engineers and to international standards ISO 14644 and EU GMP. Cleanroom validation tests to be carried out at your facility can include:

Clean rooms must be validated prior to operation. This process ensures that the clean room is working correctly. Specific standards set the requirements for clean room validation. These include ISO 14644-1 or FED 309E. After a clean room is validated and becomes active it must regularly be checked in order to ensure that it continues to meet initial standards. Specific standards list the time intervals at which clean rooms should be tested and the minimum requirements a clean room must meet. Clean Room Tests / Clean Room Validation · Air Supply and Extract Quantities · Pressure Differential Between Areas · Air Movement Control and Recovery · Airborne Particle Concentrations Optional Tests Used in Clean Room Validation · Lighting Levels · Temperature · Humidity · Heating and Cooling capabilities of the room The microbiological, bio-technological & pharmaceutical sectors are subject to GMP requirements, with testing & validation of clean room ventilation as one of the most critical parameters. We prepare necessary protocols, perform the tests & make the final reports. Our experience with meeting the stringent requirements within the microbiological, bio-technological & pharma sectors can with advantage be transferred to other industries, such as hospitals, electronics, the food sector & the device industry. As an independent testing and certification agency, we use only the most reliable and accurate testing instrumentation, calibrated to national standards.

Located in Vadodara (Gujarat, India), we are involved in rendering cleanroom validation services. Validation of the cleanroom is an important task that should be carried out by a professional. Our team is experienced in rendering the validation service as per the precise needs of the clients. We cater to different industries and conduct the validation service without creating any hassle. Moreover, our services are pocket-friendly.

validated cleanrooms are validated to a required class of cleanliness. The level of cleanliness chosen is driven by user requirements. Cleanroom classes are defined in ISO1464-1: A constant monitoring program is required after certification. Requirements for compliance are found in ISO 14644-2. Statistical analysis for cleanroom parameters is encouraged as a tool for monitoring the cleanroom after certification to ensure compliance. The tool of choice is statistical process control, SPC. Methods for evaluation and measurements for Certification are specified in ISO14644-3. It calls out for the following ten tests.  Air flow Test & ACPH Calculations  Installed Filter System Leakage Test (using PAO)  Non-Viable Particle Count Test  Recovery Test  Air Flow Pattern Test (Using Water Fogger)  Air Pressure Balancing  Containment test  Temperature & RH Measurement  Light Intensity Measurement  Sound Level Measurement Once certified to a particular class the cleanroom factors are monitored to ensure that parameters have not drifted, or changed and that the environment is under control

  UIL is a name that can be trusted for carrying out cleanroom validation requirements throughout Delhi, India. With our services, we focus on factors like temperature, airborne particulates, microbes, relative humidity, differential pressure, and air flow. Cleanroom validation is performed for a variety of reasons and we offer solutions for all of them. So, appoint us as your cleanroom validation service provider and avail the benefits of prompt and dependable solutions. Ring us on the given numbers for a detailed discussion.  

We offer a broad range of Environmental Monitoring Services for Clean rooms and can also provide you with customized monitoring programs to fulfil your needs. Complete cleanroom maintenance and cleaning service is available from Envision. This includes all HVAC (heating, ventilation, and air conditioning) servicing, filter replacements and periodic cleaning. We use a containment system to enable us to carry out works within a clean room without disturbing the controlled environment. Some of our Services for Cleanroom and BSL projects include : Airborne Particle Count Monitoring Bacterial Count determination in air under specific operating conditions HEPA Filter Integrity Test Air Flow Visualization Study OT Room Validation in Hospitals as per NABH Guidelines AMC Services of OT Rooms HEPA Filter Leak Test Velocity measurement DOP/AOP count Light Intensity UV Light Intensity Sound Level Test IQ, PQ,DQ,OQ

• Name: ISO 14644:1:2015
• Application: 60 to 70 Sq. ft per Kg.

Details Air Velocity & Air Changes (ACPH) Particle Count Test Filter Integrity Test (Using PAO) Recovery Test / Sweep Test Air Flow Pattern test (Smoke test) Temperature Mapping

• Usage: Clean room environment
• Name: clean Room Validation
• Product Name: Validation
• Quality: Q.A. / Q.C.
• Testing Machines: Calibrated
• Documentations: DQ, IQ, OQ, PQ.
• Quality: Accurate
• Test report: Thermal prints
• Management: Sterile area
• Performance by: Well trained engineers
• Service Delvery: On time
• Work policy: Disciplined
• Dress: Using own gowning

Cleanrooms are validated and then certified to a chosen class of iso 14644-1. Each class of iso14544-1 has its unique requirements that must be made for a facility to be classified in the specified classification. Cleanroom validation is performed including air flow test, filter integrity test, non-viable particle count, area recovery test, visual air flow patent. Lux and sound measurements of all clean room, laminar air flow (vertical horizontal), dhs, pass box and warehouses.

We are leading service provider for hvac/clean room validation in pharmaceutical, biotechnology,Api manufacturing company across the world as per iso 14644:2019, 14644:2015,14644:2005 and EUGMP-WHO

• Brand Name: PERFECT AIRCON

We are offering validation. *velocity test *air pressure balancing *dop / pao test *particle count test *videography.

Deeply rooted in Hyderabad (Telangana), we are an organization that is instrumental in offering excellent cleanroom validation services to the clients at reasonable charges. Our professionals make sure that the specifications of the clients are accurately met while providing the application for clean room validation. In addition, we ensure timely execution of the validation plan for the customers’ convenience. Thus, you can rely on our professionals for providing high-class services. So, contact us for optimum and affordable solutions for clean room validation any time.

We are the leading service providers of Cleanroom Validation from North India & Haryana. Clean rooms must be validated prior to operation, and this process ensures that the clean room service is working accurately. There are specific standards that set the requirements for clean room validation.

Air Velocity Measurement Air Changes Per Hour Calculation Hepa Filter Integrity Leakage Test Air Born Particle Count Test Recovery Time Test Air Flow Pattern Test

We are providing validation. When a validation project is planned, it is much easier for validation engineers to prepare the work.

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