No. VertiMotion supports structured physical execution, observation, and documentation. Screening, diagnosis, protocol selection, interpretation, and follow-up remain under appropriate clinical oversight.

Operation should be performed by trained staff under the clinic's governance model and supervising clinician pathway. Operator scope should follow local professional and regulatory requirements.

A recommended room of at least 18 m² is preferred, with a practical operating area around 10 m² and platform footprint around 6 m².

The reference setup is AC 220V / 50Hz with a 1600 VA power rating and UPS support.

Published BPPV evidence includes Shan et al., The Laryngoscope, 2015, reporting 132 patients treated with computer-controlled canalith repositioning. Published short-term study data should be reviewed independently and does not guarantee outcomes.

VertiMotion supports clinic room deployment, managed dizziness programs, and co-branded dizziness centre discussions depending on room fit, governance, demand, and strategic ambition.

Partnership structure is discussed case by case. Some pilots may focus on managed program or partnership models rather than a simple equipment purchase conversation.

A pilot usually confirms interest, assesses room suitability, reviews regulatory and clinical pathway requirements, builds a referrer education plan, defines operating metrics, then launches with review cadence.

ENT, vestibular rehabilitation, physiotherapy, GP / multidisciplinary clinics, private hospitals, and strategic clinic groups are the core fit.

We review clinic fit, assess room and workflow requirements, then discuss the most suitable partnership model.