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HCL Technologies

Process Validation

Process Validation

Over the recent years, the Process validation activity is being taken seriously in the medical device industry. and following this approach is considered as a strong tool for ensuring the quality of process is kept in a high limit and products manufactured with high quality. The Process validation directly contributes to the quality of the product by the minimizing the defective products and overall it contributes to the Patient safety. This paper will make you understand and guide to successfully validate the process to adhere US FDA and European requirements.

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HCL provides software and services to U.S. Federal Government customers through its partner ImmixGroup, Inc. Please contact ImmixGroup, Inc. at HCLFederal@immixgroup.com

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