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Services - Validation & Qualification
     
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. The desired results are established in terms of specifications for outcome of the process. Qualification of systems and equipment is therefore a part of the process of validation. Validation is a requirement of food, drug and pharmaceutical regulating agencies such as the US FDA and their GMP guidelines. Since a wide variety of procedures, processes, and activities need to be validate.

HVAX is a global player for validation services. Experienced team at HVAX carries out cleanroom validation services using calibrated sophisticated equipment’s, as HVAX team has a major experience in pharmaceutical sector, SOPs are generated and strictly followed for validation purposes. The reports generated are in appropriate formats thus very clearly giving an idea to client on non-compliances, if any ,considering the global acceptable standards.