yo alex, i’m in biopharma and the data verification regulatory means are a nightmare. it’s like, every time we think we’re done, there’s another audit or checklist.
we’ve been using labware lims and it’s been a lifesaver. still a lot of work, but at least it’s organized.
do you think these regs are here to stay? or will they ease up eventually?
we’ve been using labware lims and it’s been a lifesaver. still a lot of work, but at least it’s organized.
do you think these regs are here to stay? or will they ease up eventually?