Having a good validation system, reduces the risk of Regulatory Non-Compliance.
Validation is a method to establish documentary evidence demonstrating that a process, procedure, or activity carried out in testing and the results are fully compliant to the industry regulations. In simple terms, validation is determining if the system complies with the requirements and performs functions for which it is intended and meets the organization’s goals and user needs. In pharmaceutical industry, the product must give surety that it will give consistently produce expected results.
Unicorps is a niche player for cleanroom validation services. Our team is highly skilled and experienced to carry out cleanroom validation services using the calibrated sophisticated equipment. The reports generated gives a clear picture to the client on non-compliances, if any,considering the globally accepted regulatory standards.
We validate and qualify every system that’s part of our offering. From different sampling zones to big warehouses, Unicorps ensures that Direct air flow zones, Laminar Equipment, Cold-rooms, Stability chambers, and Clean rooms are properly validated.
We're Gentle in our sales method, so we don't push our people to push you. You won't find us trying to endlessly upsell you, or force upon you only the products that we manufacture. We work with a network of both affordable and world-class brands. The project coming to realization is more important than anything else and we work to bringing that dream to fruition. To understand how we can find the right mix, click below to schedule a call with you.
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