GROW-Service qualifies as a Class I medical device under the definitions of Council Directive 93/42/EC.

The following documentation supports the Manufacturer's Declaration of Conformity to the requirements of the directive.

Declaration of Conformity
Registration with Medicines & Healthcare products Registration Agency
Technical Information and Specification
Risk Assessment and Mitigation
Clinical Evidence of Effectiveness
Documentation to support developers and managers of API implementation
GROW-Service Web Application (UK GROW-App)