KVAi

Data processing agreement

This describes how KVAi processes material on an agency's behalf. It is written to be attached to the terms of use, and its factual annexes are generated from the product itself so they cannot drift out of date.

Roles

The agency is the controller. KVAi is the processor. Where the agency is itself processing on behalf of a pharmaceutical client, KVAi is a subprocessor to that arrangement — which is usually the shape of the relationship in practice, and is why the annex below matters to the client's own legal team.

Annex 1 — subject matter and duration

Drafting, editorial checking and reference work on promotional and educational material for medicines, for as long as the agency holds a workspace.

Annex 2 — nature and purpose

Annex 3 — categories of data

Predominantly commercial and scientific material rather than personal data: summaries of product characteristics, clinical publications, claim matrices, house style guides and draft copy. Personal data is limited to the names, work email addresses and actions of the agency's own staff.

KVAi is not intended for patient data. The product has no clinical or patient record function, and material of that kind should not be uploaded.

Annex 4 — subprocessors

The current list, with what each receives and where, is published and kept current at https://kvai.co.uk/legal/subprocessors.

Annex 5 — security measures

These are the measures actually implemented, not aspirations:

Annex 6 — return and deletion

An owner can request deletion of a workspace, which removes everything in it after a grace period. Documents withdrawn from a client space are excluded from retrieval immediately, so they can no longer be cited.

Assistance and audit

We will help with data subject requests, and provide the information needed for a controller's own impact assessment. What is left after an erasure is documented in the product so it can be answered consistently.