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.



To know more: https://dreamsoftindia.com/industrial-automation-software-development.asp

Contact Us on: +91.9870310606/ 7710013322

Email Us on: sales@dreamsoftindia.com

#Dreamsoft #industrialautomation #automation #plc #OPC #automationsoftware #automationsolutions #automationsystems  #iiot #iot #softwaredevelopment #automationsoftwaredevelopment #industrialautomationsoftware #applicationdevelopment #iotapplication #datalogging #dataanalysis #reportingsoftware #automationsolutions #homeautomation #scadasolution #scadasoftware #wincc #plcsolution #hmisolution #industrialpc #opcinterfaceapplication #opcserver #part21CFR #protocols #datalog #dataloggingsolution #hmisolutions #batchreporting #autoclavesolution #pharmasolutions #TCP #IP #Deviceinterface #devicesoftware #customizedsoftwared #opchda #opcda #opcua #driversoftware #controllerdevice #usermanagement #scadausermanagement #scadauser #scadamanagement

Comments

Popular posts from this blog

How to Regulated Industries requires all Windows User Management Activities to be Audited with Report.

Pharma Tech/Lab Tech Expo 2024 Visit Us 8/9/10 August Helipad Ground - Gandhinagar-Gujarat- Hall No 10-Stall No B37

DreamSoft's Zelenka Reporting Application Installation - Water Domain in Pharma & Biotech Companies.