For our Esteemed System Integrators and OEM partners of Industrial Automation Software Application
21 CFR Part 11 Allows the Industry to use Electronic Records and Signatures alternatively to paper records and Hand-written Signatures.21 CFR is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Compulsorily used in the Pharma Industry, DreamSoft has achieved full compliance in Industrial Software Application with 21 CFR.
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