Labs and institutes with no software team
You run studies, not software projects. We build the system, host it and keep it running, so nobody on your staff has to become the IT person.
Andolasoft builds research participant tracking software around the way your study runs: enrolment, consent and visits in one place. It is made for labs with no software team, and we keep running it after launch.
Figures describe one platform we built for a US research institute. The client is not named.
Andolasoft builds custom participant tracking systems for research studies. The system keeps one record per participant for enrolment, consent and visits, and replaces the spreadsheets and shared drives a study team would otherwise use. Each person sees only what their role allows, and changes are logged. Andolasoft hosts and maintains the system after launch, so the lab does not need its own software team.
The same four jobs your coordinators do today, without the copying, checking and chasing.
| Task | In a spreadsheet today | With a tracking system |
|---|---|---|
| Enrolment | One shared file that several people edit, with no record of who changed what. | One record per participant, with a status everyone sees and a history of changes. |
| Consent and re-consent | A column of dates, checked by hand before each visit. | Consent status sits on the participant record, and the system flags who needs to re-consent. |
| Visits and follow-ups | Calendar entries and reminder emails kept by one coordinator. | A visit schedule per participant, with reminders and a list of what is overdue. |
| Reporting | Numbers copied into a new sheet each time a sponsor or committee asks. | Recruitment and status counts pulled from the same records the team works in. |
You run studies, not software projects. We build the system, host it and keep it running, so nobody on your staff has to become the IT person.
More participants, more coordinators or a longer follow-up period than a shared file can handle safely.
Each study keeps its own participants, schedule and access rules, and your team works in one place.
You stay in control of what the system does. We do the building and the running.
We go through your current spreadsheets, forms and steps with the people who use them, and write down what the system must do.
We build the first version around a single study, so your coordinators can try it with real work before anything else moves.
Existing participant records are brought in from your spreadsheets and checked with your team.
We host, monitor and update the system after launch, and change it when your study changes.
Participant records are personal, and often health information. These are the controls we design in from the start.
Each person sees only what their role needs. A coordinator, an investigator and an administrator do not get the same view.
Changes to participant records are logged, so you can answer who changed a record and when.
The system can run on cloud infrastructure built for protected health information, or on your institution’s own servers.
In our research institute project, data is encrypted between the apps, the coordinator portal and the server.
See how that project was builtThe full list, and what we do not claim, is on our security and data handling page. For how Andolasoft itself handles personal data, see our privacy policy.
A custom system does not have to replace everything. It covers the gaps your current tools leave.
Many labs collect study data in REDCap. A custom tracking system can sit next to it and cover what your team still does by hand, such as scheduling, reminders or a participant app.
About REDCapYou do not start from an empty system. Current participant lists and visit logs are brought in during setup.
When participants need to log data themselves, the same system can include iOS and Android apps, as it did for a US research institute.
Read the case studyA biological research institute needed to collect daily health data from study participants. We built one platform for participants and coordinators.
Participants log food, sleep, exercise and medication each day. The apps keep working without a signal and sync later.
Research coordinators review logged data, photos and survey responses in a web portal.
The apps, the server and file storage run on infrastructure built for protected health information. Health data from Apple HealthKit and Google Fit is read only with each participant’s consent.

A practical checklist for keeping consent and enrolment records that are easy to find and explain. Your IRB still sets the rules for your study.
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A seven-step guide for research labs with no software team: map your spreadsheets, fix the rules, pick a route, migrate safely and hand the system an owner.
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A ten-point checklist for a research lab to check who can see participant data, whether changes are logged, and what to ask before you trust a study tool.
Read articleWe will look at your current spreadsheets and steps, and tell you what a tracking system for your study would cover. You will hear back from a solutions architect within one business day.
We can sign an NDA before the first technical conversation.