Hello
Greetings...
I am a Software validation expert from India. I have more than 8 years of experience End to End GxP regulatory requirement for software, 21CFR part 11, 21 cfr part 210 and 211, equipment validation , computer system Validation (Preparation of URS, Risk Assessment, DS, IQ, OQ, PQ, TM, VSR), SOP Writing, QA, QMS Documentation. I have worked with many Pharma companies like CIPLA, Torrent Pharma strides shasun, and amenal pharmaceutical, as validation consultant
I understand your requirements and I can help you to execute this project. looking forward to work on this project.
I am available for Skyp interview.
regards
Anam