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What is Validation?

Validation is the process of establishing documentary evidence demonstrating that a procedure, process, or activity carried out in testing and then production maintains the desired level of compliance at all stages. In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products, it is also assured that the process will consistently produce the expected results.
Our validation services include strategic planning of validation, commissioning and qualification activities which includes process validation, clean room validation and area validation, our validation approach is based on current WHO, GMP, EU & USDA regulation and executed according to user's requirements, specification and SOP's.
We provide temperature, humidity mapping services for clean rooms, cold rooms, refrigerators, freezers, warehouse, stability chambers, incubators, oven, tunnels, autoclaves, dry heat ovens hot air ovens & muffle furnaces widely used in the field of pharmaceutical, hospitals, blood banks, tissue labs, metrology, & electronics etc.

Validation Services

Tests
  • Air Velocity Test
  • Hepa Integrity Test
  • Particle Count Test
  • Recovery Test
  • Air Flow Test (Includes videography)
  • Containment Leak Test
  • PLC Validation
Compressed Air Validation
Pure Stream Validation
Thermal Mapping For:
  • Autocloves, Superheated autocloves
  • Tunnels, Incubators/Bod Incubators/Bacti-Riological Incubators
  • Lyophilizer, Ovens & Waterbaths
  • Area Mapping, Warehouse Mapping