ABSTRACT
Air pressure gradient from weighing cabin → corridor: 3.3 4.14 Dust extraction systems available? 5.11
Operations:
4.15 Balances regularly calibrated? 3.41 4.16 Only pharmaceutical raw materials in this area? 5.17 4.17 Check on remains from previous materials before entering of
new materials into a weighing cabin? 5.9/5.35
4.18 Only one material in one cabin? 5.9 4.19 Are dispensed materials correct labeled? 5.29 4.20 Only released products in the dispensing? 5.31 4.21 Cleaning SOPs for the dispensing? 4.28 4.22 Previously dispensed material recorded on weighing
protocol? 4.8
4.23 Safety measures against mix-ups during assembling (e.g., cage pallets)?
