Picomto complies with the requirements of the regulations FDA 21 CFR Part 11 Annex 11 / GMP
“If it’s not written down, it didn’t happen” »
With Picomto, sleep tight !
“Who is allowed to enter data ?”
“Who is allowed to modify data?”
“How do you know who enter data?”
“How do you know which data has been modified?”
“When do you lock the data input?”
“Can you do the following actions ?”
“Can you show the validation activity results?”
“Does the validation include: success / failure, signature, date / time ?”
From now on, you can answer these questions in 1 click.
What benefits ?
A guarantee to generate and maintain 100% FDA compliant digital data.
During inspections, generate the required reports in a few clicks.
An exploitation of your FDA work instruction on all devices (computer, mobile, tablet, A/R).