COVID forever changed how firms view their internal protocols and procedures. It affected companies of all sizes and industries, posing new obstacles for staying connected. The pandemic demonstrated that all firms need to integrate digital instruments into everyday routines. They became important for far more than hybrid working models.
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Rob Packard from Medical Device Academy introduces the newest procedure, SYS-051, for software tool validation. Written by Mary Vader, this procedure is specifically for software tools utilized in quality systems. It is separate from the existing software validation procedure. The video takes viewers through the procedure, highlighting references to requirements, inputs, outputs, and revision history provided within SYS-051.