A Site Acceptance Test (SAT) is the qualification stage followed by the Fats and it features a number of testing accomplished on products, carried out in the proprietor consultant site.
Planning for Procedure: Ensure that the equipment is entirely All set for manufacturing, with all necessary configurations and changes completed.
Tip: Use tables to list equipment and options necessary for each test, building preparation clear-cut for personnel.
In predicaments like these, the Operator may well contact back again the contractor to fix it, but only whenever they appreciate the look intent and its impact on performance.
Install PLC controllers And that i/O modules in accordance Using the process configuration and installation pointers.
The distinction between a site acceptance test along with a factory acceptance test is an SAT is executed at the customer’s site, although a Fats is done with the company’s manufacturing unit.
SAT minimises challenges related to machines failure and integration issues. It safeguards investments and makes sure generation readiness by verifying:
Why It Issues: A glossary increases comprehension by clarifying specialized phrases and acronyms utilised through the document.
A visual Test entails analyzing the physical site making sure that it satisfies the necessities laid out in the venture documents. This will incorporate checking for journey hazards, correcting signage, and making sure which the creating is in great site acceptance test checklist repair.
Also, another reason to visually confirm is usually that from time to time, elements get broken through transportation and logistics. So, it's important to check the system initial before beginning it.
In addition, an SAT is used to confirm the system fulfills The shopper’s needs and will be operated in The client’s setting. Meanwhile, a Extra fat is employed to verify the program meets the contractual demands and will be operated in the vendor’s manufacturing facility ecosystem.
Basically, the SAT makes sure all managing and manufacturing of medicinal products and solutions meet up with the expectations of confidence the laws agreements count on them to help make.
Validate the generation and Screen of system occasions, read more for example equipment malfunctions or status adjustments, about the graphical interface.
Documentation – Document and evaluate test final results to find out If your process fulfills the essential specs.