EMPOWERING DISCOVERY

Where research lives

A next-generation data collection platform that allows you to create highly customisable studies in minutes. It's more than just a siloed tool, it's a place to run every study you manage, see what other researchers are working on, and collaborate with them.

Taking part in a study? See what Indacas means for you

A platform built for
research at every scale

Everything you need to run a study, manage your team and keep your data clean and compliant.

Everything else that's included

How it works

Tell us about your project and we'll match you to the right tier. Pay monthly while you're active, pause anytime and your data stays put.
  1. 01

    Complete the study wizard

    Tell us about your proposed project, its length, expected participant count, number of responses and the type of data you'll collect.

  2. 02

    Get a tier suggestion

    We match your needs to the right tier so you only pay for what your study actually needs.

  3. 03

    Pick a tier and pay monthly

    Choose your tier, pay monthly, and start collecting data straight away. No long contracts, no setup fees and no variable pricing based on project funding.

  4. 04

    Pause anytime, your data stays

    Stop paying and your study goes dormant. Study custodians can still access their dormant study to export all of the data. Simply reactivate your subscription to resume collecting data.

Ready for the scrutiny
your study will face

Encryption, role-based access, audit trails and versioned consent are built in, so your information governance and ethics submissions describe what the platform does rather than what you plan to build.

Secure

Protect sensitive data with encryption, role-based access and full audit trails.

2FA

Require two-factor authentication within your study for all researchers with the click of a button in your study settings.

Documents

Once you have created a study, download an Indacas DPIA which is filled out based on how the study is setup.

Compliant

Designed to support regulatory and institutional requirements with consent flows, retention controls and audit ready exports.

Indacas is already helping people

We’re immensely proud of the studies that are already being powered by Indacas. These studies are engaging thousands of participants to accelerate breakthroughs, uncover new insights and advance global scientific goals. Read more below:

COLO-SPEED

Colospeed logo
by Colospeed
Our aim is to stop people dying of bowel cancer. Bowel cancer, also called colorectal cancer (CRC), is the fourth most common cancer and the second most common cancer death in the UK. COLO-SPEED (Colo...

DM Patient Registry

Colospeed logo
by The UK Myotonic Dystrophy Patient Registry
For the treatment of Myotonic Dystrophy, promising new therapeutic strategies are currently being developed which need to be tested in clinical trials/research studies. This registry will make the rec...

Adult SMA Reach

Adult SMA Reach logo
by Adult SMA Reach
Adult SMA REACH (Research and Clinical Hub) is a data collection study aiming to gain a better understanding of the impact of standards of care and new treatments on the natural history of Spinal Musc...

FSHD Patient Registry

FSHD logo
by The UK FSHD Patient Registry
This registry is for patients living in the United Kingdom who are affected by Facioscapulohumeral dystrophy (FSHD type 1 or 2), with no age restrictions. This registry is primarily designed to collec...

DMD Hub

DMD Hub logo
by The DMD Hub
The DMD Hub Site Feasibility and Clinical Trial Database is part of the DMD Hub tools and services offer, allowing colleagues at DMD Hub clinical trial sites to provide and store information about the...

UK SMA Patient Registry

UK SMA Patient Registry logo
by UK SMA Patient Registry
Spinal muscular atrophy (SMA) is a rare neuromuscular disorder. The small number of individuals affected by SMA presents a challenge to the study of the disorder and the understanding of the impact of...

Sjögrens Registry

Newcastle University
by Newcastle University
The United Kingdom Primary Sjögren's Syndrome Registry (UKPSSR) is a national research biobank of people with Primary Sjögren's Syndrome.

Common questions

Here are some of the most common questions Indacas users want to know. Still have a question? Ask us
How long does it take to set a study up?

Create your study, pick a tier and you can be collecting data in minutes. Every tier starts with a free trial and no payment card, and there is no implementation project or setup fee.

Is Indacas open to people outside of Newcastle University?

Yes, everyone is welcome to use Indacas.

Can we host the system on our own servers?

Indacas is UK hosted and all data is encrypted and auditable. It's not possible to run your own localised system.

Can we transfer our existing data?

Yes, please get in touch with us if you need to transfer legacy data into your Indacas study.

Is this platform only for studies with participants?

No, our studies have specifically been designed to be extremely robust and customisable so that any data collection project can make use of them.

Where is data stored?

All data is stored in the UK. In the future all data will be stored in the country of residence of the study.

Is Indacas GDPR compliant?

Yes. Indacas is built around UK GDPR requirements. Studies must declare a lawful basis for processing, and our consent flows capture and version every consent decision so you have a full audit trail. Participants can withdraw consent and request deletion of their data at any time, and study custodians can fulfil subject access and erasure requests directly from the platform.

Can we export our data?

Yes. Study custodians can export all of their study data to CSV at any time, including while a study is dormant.

Can participants manage their own data?

Yes. Participants have a dashboard for each study they are enrolled in, where they can view and update their own records, revoke consent, and request that their data be deleted. Consent and access are managed on a study-by-study basis, so a participant can stay active in one study while withdrawing from another.

Can studies access participant data from other studies?

No, a study can only see what you provide them. There is no way for a different study you join to access that other studies data.

How will we be charged?

Studies will be charged for monthly across three tiers which vary in price based on usage and features.

What happens when we stop paying for a study?

All of your data will still be accessible and exportable by the designated custodian. However, you will be restricted from other actions on the data within the study until it's made active again.

Get in touch

Do you have a question we haven't answered? Get in touch and we'll get back to you as soon as possible.