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Vivalink pricing

No price is published: no pricing page, unit of charge, range, tier, implementation fee position or minimum commitment, and sales start from a contact form. The company sells a development kit, a sensor family and a data platform to organizations building their own monitoring products, an audience that has to model cost of goods before committing engineering effort.

Pricing terms

How Vivalink pricing works

Pricing model
Not disclosed. No unit of charge is described anywhere. The offering combines reusable hardware sensors, consumable adhesives, edge routers, a cloud data platform and a development kit, and nothing indicates whether charging follows the sensor, the monitored patient, the data volume, the seat or an enterprise license, nor how the clinical and clinical trials markets price relative to one another.
Implementation
Not disclosed. The company describes a self serve integration path: a development kit covering sensors and data services, edge tools for building and testing mobile applications, routers for on premise multi patient monitoring and web services for cloud integration. Whether integration support, validation assistance or documentation for a customer's own regulatory submission are charged separately is not stated; for research customers, system validation under 21 CFR Part 11 is part of the work.
Business associate agreement
Not published as a template or posture. Vivalink names three regimes. United States health privacy law and European data protection law are both claimed, alongside the federal rule governing electronic records and electronic signatures in regulated research, which imposes requirements on record integrity, audit trails, system validation and attributability and is what a trial sponsor must satisfy for data to be admissible to a regulator. The international information security management standard is also listed. The contractual layer is not published: no agreement template, execution requirement, negotiation stance or subcontractor position. Customers build their own applications and hold the patient relationship, so where Vivalink sits in the contracting chain matters, and the company does not say whether it contracts directly with covered entities, sits as a subcontractor to the application developer, or handles only de identified streams. That position decides how an integrator states its own compliance position downstream. Whether the platform handles identified data by default is also not stated.

The footer links a product warranty, an end user license agreement and license terms for developers and solution partners, which govern use rather than price. Reusable sensors, consumable adhesives, a recurring data service and a development kit could each be charged differently, and a trial sponsor running a fixed study and a hospital at home program running continuously consume very differently. The unit of charge, whether sensors are bought or leased, the platform licensing basis and the difference between trial and clinical pricing are not published.

Compared on price

Vivalink pricing against its alternatives

Published prices for Vivalink and the products closest to it. Each figure is as the vendor publishes it, in its own currency and billing unit.

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Questions

Vivalink pricing, answered

How much does Vivalink cost?

Vivalink does not publish a price. The company sells a development kit, a sensor family and a data platform to organizations building their own monitoring products, an audience that has to model cost of goods before committing engineering effort. The footer links a product warranty, an end user license agreement and license terms for developers and solution partners, which govern use rather than price.

Does Vivalink charge an implementation fee?

Not disclosed. The company describes a self serve integration path: a development kit covering sensors and data services, edge tools for building and testing mobile applications, routers for on premise multi patient monitoring and web services for cloud integration. Whether integration support, validation assistance or documentation for a customer's own regulatory submission are charged separately is not stated; for research customers, system validation under 21 CFR Part 11 is part of the work.

Does Vivalink offer a business associate agreement?

Not published as a template or posture. Vivalink names three regimes. United States health privacy law and European data protection law are both claimed, alongside the federal rule governing electronic records and electronic signatures in regulated research, which imposes requirements on record integrity, audit trails, system validation and attributability and is what a trial sponsor must satisfy for data to be admissible to a regulator. The international information security management standard is also listed. The contractual layer is not published: no agreement template, execution requirement, negotiation stance or subcontractor position. Customers build their own applications and hold the patient relationship, so where Vivalink sits in the contracting chain matters, and the company does not say whether it contracts directly with covered entities, sits as a subcontractor to the application developer, or handles only de identified streams. That position decides how an integrator states its own compliance position downstream. Whether the platform handles identified data by default is also not stated.