What details regarding an Automated Dispensing Device must be reported to the Drug Control Program?

An Automated Dispensing Device (ADD) plays a crucial role in modern pharmacy practice, particularly in streamlining medication dispensing and enhancing inventory management. In Massachusetts, reporting pertinent details about these devices to the Drug Control Program ensures compliance with regulations and promotes patient safety.

The correct choice encompasses all relevant information that must be reported: the manufacturer’s name and address of installation, as this helps regulatory bodies track the devices and ensure they comply with safety standards; the device's location and facility name, which is essential for pharmacy inspections and audits; and the model of the device, which aids in identifying any specific concerns or recalls related to that particular model.

Each of these details serves a significant purpose in maintaining oversight of pharmaceutical care facilities, preventing misuse or malfunction of the devices, and supporting the state’s efforts to regulate medication dispensing accurately. Thus, it is imperative to report all these particulars to the Drug Control Program, ensuring an organized and accountable pharmacy practice environment.