Cleanroom Validation Solution

On-Site Calibration & Validation Facility

Cleanroom validation solution (CVS) is long established as one of the leading cleanroom validation, Equipment qualification, Temprature mapping services provider company in india. We provide an extensive range of cleanroom validation, Equipment qualification, Temperature mapping services with all testing carried out to the highest standard by fully trained and competent engineers.
Our Cleanroom Validation & other validation / qualification methods precisely comply with Regulatory bodies like ISO 14644:2015 and guideline agencies such as MHRA, FDA, EU GMP, WHO-TRS-961, WHO-TRS-937, EN285 and Schedule M for all room classification and so many other Industry-Specific Standards.
Cleanroom validation solution (CVS) has expertise not only in Pharmaceutical cleanroom but Operation theatre, Laboratory, and Various equipment like Bio-safety cabinet, Laminar air flow equipment, Fume cupboard, Local Exhaust Ventilation (LEV) system or relocation of equipment.

Temperature Mapping of storage area (retain sample room, control sample room, RM store FG store, quarantine
About Us

Who is Cleanroom Validation Solution?

Since our incorporation in this industry, we have been steady in providing a superior quality array of products in accordance with the requirements of our clients.

We upgrades the knowledge and skills of our personnel through continually inline with regulatory guideline and training to make sure continuous Human Capital Success.

Following are some of the reasons of our success:
- Strong focus on quality compliance.
- Timely delivery of physical service and support.
- Provide effective document as per international guideline.
- Physical presence and urgent document support provide during critical audit.
- Service with answers “today” is our credo to support you with a fast and reliable service by specially trained service engineers to serve your specific needs.

Why We Are?

Why Are You Choose Us?

  • Onsite Facility for validation / Qualification / Temperature Mapping Services.
  • Qualified and Well Trained Engineer / Technician Team
  • Quality assurance department for exhaustively reviewed All reporting and documanrtation work thoroughly reviewed as per regulatory guideline
  • We have Separate Quality Assurance and Documentation Department to accomplish clients all complicated activity on urgent basis during Audit.
  • All Reporting work complies National / International and Major regulatory body like USFDA, MHRA, MCC,TGA, WHO, FDA, ISO etc
  • Our motto is punctual Services and Fast Reporting work with in very sort time.
  • On-Site Calibration & Validation Facility.
  • Remind Customers for due date of Equipment Validation activity by Mail/Telephonic/SMS.
Our Services

Our Validation Services Include

  • Temperature mapping of...

    Walk in stability chamber Humidity chamber Cold chamber Cold room Deep frezer Refrigerator Incubator BOD incubator Heating block HOT air oven / Vacum oven Storage area (retain sample room, control sample room, RM store FG store, quarntine)
  • Validation (Thermal Mapping) of...

    Deprogenation tunnel Dry heat sterilizer Autoclave (Vertical/Horizontal) Steam sterilizer Bung processor Storage vessel Filling machine SIP Storage vessel SIP Lyophilizer (Shelf uniformity / SIP)
    Lyophilizer Qualification
  • We provide testing & validation of Cleanrooms validation

    Heating and ventilation air controling unit (HVAC/AHU) Laminar Air Flow (LAF) / Reverse Laminar Air Flow Unit (RLAF) Bio Safety Cabinets Dispensing/Sampling Booth Garment Cubicles Dynamic Passbox Isolators HEPA filter Close restricted access beriar system (CRABS) Open restricted access beriar system (ORBS) Depyrogenation tunnel / Dry heat sterilizer
  • Other Services

    Air Velocity Measurement and & ACPH Calculations PAO HEPA Filter Integrity Test Non viable Particle Count Test Airflow Visualization Test & Videography Recovery Test Temperature & RH Measurement Light Intensity Measurement Sound Level Measurement
    1.HVAC & Cleanroom validation (Air velocity & Non viable Particle Count Test )
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Our Ambition

Our Ambition Is Our Main Motto

To perform the cleanroom validations, Equipment qualiifcation and thermal mapping activity of area and equipment traceable to international standards and make feel customer pleasant with regulatory audits like as WHO, USFDA, TGA, MHRA, EU, PICs, MCC, Schedule M Etc. by convention the requirements of mandatory tests, test methods and documentation as per the regulatory guidelines and the above regulatory bodies.


We feel pleasure to bring to the awareness of our client about the conditions of their Cleanroom, aseptic area, temperature mapping of area, Equipments validation and Measuring Instruments by caring out test with high accuracy, which plays very important role for meeting the institutional Quality policy.

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