About Us
Aspire Quali-Tech - ‘Aspire To Build Quality System ’ Is Providing Services For Complete Environment Monitoring Systems To Various Industries Like Pharmaceutical, Chemical, Healthcare, Environmental Monitoring, Food Industry, Engineering, Research Institutes.
Leading Service Providers for Complete Environment Monitoring Systems To Various Industries
About UsContact Info
- 108, Panchvati Plaza, Plot No. 95-96 Sector-5, Ghansoli Navi Mumbai 400701, India
- +91-9892022757
- aspirequalitech@gmail.com
Clean Room and HVAC Validation Services In Mumbai- India.
Aspire Quali-tech offers following services:
PARTICLE COUNT TEST AIR VELOCITY, ACPH CALCULATIONS
HEPA FILTER INTEGRITY TEST
RECOVERY TEST
PRESSURE BALANCING TEST
AIR FLOW PATTERN
Clean room and HVAC (Heating, Ventilation, and Air Conditioning) validation are critical processes in various industries, particularly those that require controlled environments such as pharmaceuticals, biotechnology, healthcare, electronics manufacturing, and food processing.
Clean room validation ensures that the environment within a controlled classified area meets specified air quality standards to maintain product quality, prevent contamination, and ensure safety.
Particle Counting: Measures the concentration of airborne non -viable particles in different size ranges.
Airflow Patterns: ensures that air flows in a controlled manner to prevent cross-contamination.
HEPA filter integrity testing ensures that the HEPA filters are intact. Checks the efficiency of air filters in removing particles and contaminants.
Air velocity measurement is ensuring proper airflow and adherence to cleanliness standards.
Microbial Monitoring: Checks for the presence of microorganisms in the environment.
Temperature and Humidity Control: Maintains stable conditions to meet product requirements.
Testing and Balancing: Adjusts airflow rates and temperature settings to achieve optimal conditions.
Clean room validation often follows guidelines from regulatory bodies like FDA (Food and Drug Administration), ISO (International Organization for Standardization), and GMP (Good Manufacturing Practices).
Clean Room and HVAC validations are essential for ensuring the quality, safety, and compliance of products manufactured or processed within controlled environments. It helps to maintain conditions conducive to the production of sensitive goods while minimizing the risk of contamination or adverse environmental factors
Aspire Quali-Tech fulfills the needs and expectations of the customers by providing Quality Service in a cost effective way.