CliniCore

Clinical research center management system

Free for up to 5 active studies and 3 with eSource

Synvia CliniCore: Your research center's operations, all in one place

A single system to conduct your center's studies, from visit scheduling to source data entry. Traceable and auditable at every action.

Technology from those who live the practice

Technology from those who live the practice

CliniCore was born out of the actual operations of those who conduct clinical research at scale.

CliniCore was born out of the actual operations of those who conduct clinical research at scale.

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Studies conducted

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Studies conducted

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Studies conducted

+0

Years of operation

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Years of operation

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Years of operation

+180

Industries served

+180

Industries served

+180

Industries served

+890

Employees

+890

Employees

+890

Employees

Synvia CliniCore

Synvia CliniCore

Simple to adopt. Rigorous where it matters.

Designed for the routine of those who coordinate the center and for the demands of clinical research.

Your team is operational on day one

Access it directly from your browser. Each pending item already comes with the action to resolve it.

Your team is operational on day one

Access it directly from your browser. Each pending item already comes with the action to resolve it.

Designed for coordination

Screens designed for specific stages. The day's operation in a single view.

Designed for coordination

Screens designed for specific stages. The day's operation in a single view.

Security in every record

Participants and visits by code and initials, with access by profile and audit trail.

Security in every record

Participants and visits by code and initials, with access by profile and audit trail.

One platform for the entire center's operation

One platform for the entire center's operation

All modules on a single database.

All modules on a single database.

Logistics management for clinical studies with materials control, importation, and regulatory compliance by Synvia

Study preparation

The center needs to be ready: parameterized protocol, delegated team, approved documentation.

Protocols and milestones

Parameterization, timeline, and regulatory approvals

Protocols and milestones

Parameterization, timeline, and regulatory approvals

Protocols and milestones

Team and delegation

Roles, certificates, and availability

Team and delegation

Roles, certificates, and availability

Team and delegation

Study documents

Versioned file, with approval workflow

Study documents

Versioned file, with approval workflow

Study documents

Patient recruitment

Each participant has a background, a path, and an agenda. The center follows all three from the very first contact.

Acquisition and referencing

origin of each center participant

Acquisition and referencing

origin of each center participant

Acquisition and referencing

Participant funnel

From pre-screening to study completion

Participant funnel

From pre-screening to study completion

Participant funnel

Visiting schedule

Generated by the study's parameterized schedule

Visiting schedule

Generated by the study's parameterized schedule

Visiting schedule

Logistics management for clinical studies with materials control, importation, and regulatory compliance by Synvia

Conducting the visits

The day of the visit without improvisation: the team knows what to do, what to skip, and what to record.

Overview of the day

Prioritized queue of what needs attention

Overview of the day

Prioritized queue of what needs attention

Overview of the day

Study pharmacy

Product inventory, dispensing, and accounting

Study pharmacy

Product inventory, dispensing, and accounting

Study pharmacy

Quality and compliance

Protocol deviations and adverse events

Quality and compliance

Protocol deviations and adverse events

Quality and compliance

Center tracking

Monitoring, indicators, and the financial health of the studies, gathered in one place.

Monitoring and queries

CRA visits, pending tasks, and follow-up

Monitoring and queries

CRA visits, pending tasks, and follow-up

Monitoring and queries

Center finance

Financial management of each conducted study

Center finance

Financial management of each conducted study

Center finance

Reports and indicators

The performance of the center's operation

Reports and indicators

The performance of the center's operation

Reports and indicators

Synvia CliniCore

eSource: o dado-fonte nasce digital

The research participant's electronic medical record. Data is recorded during the visit, already attributable and traceable from the source — without intermediate paper.

Digital source data, attributable and traceable from its origin

Digital source data, attributable and traceable from its origin

Integration with Synvia TrialCore's eCRF: registered once, it goes directly to the study without re-keying

Integration with Synvia TrialCore's eCRF: registered once, it goes directly to the study without re-keying

Audit trail for each record, in compliance with 21 CFR Part 11

Audit trail for each record, in compliance with 21 CFR Part 11

Synvia CliniCore

eSource: source data is born digital

The research participant's electronic medical record. Data is recorded during the visit, already attributable and traceable from the source — without intermediate paper.

Digital source data, attributable and traceable from its origin

Digital source data, attributable and traceable from its origin

Integration with Synvia TrialCore's eCRF: registered once, it goes directly to the study without re-keying

Integration with Synvia TrialCore's eCRF: registered once, it goes directly to the study without re-keying

Audit trail for each record, in compliance with 21 CFR Part 11

Audit trail for each record, in compliance with 21 CFR Part 11

Security and certifications

Security at the standard of those who are already certified

Developed by Synvia, ISO/IEC 27001 certified, with encrypted and segregated data by center, profile-based access, and an audit trail for each record.

ICH GCP

ICH GCP

LGPD

LGPD

Law 14,874/2024

Law 14,874/2024

FDA 21 CFR Part 11

FDA 21 CFR Part 11

Plans

Plans

Free for the first studies at your center

Free for the first studies at your center

It is Synvia's commitment to Brazil's research centers and to the advancement of clinical research in the country.

It is Synvia's commitment to Brazil's research centers and to the advancement of clinical research in the country.

5 · active studies under site

5 · active studies under site

3 · active studies with eSource

3 · active studies with eSource

$0 · license and per-user billing

A complete ecosystem, from source data to regulatory submission

A complete ecosystem, from source data to regulatory submission

CliniCore is part of the Synvia software family. Each platform covers a stage of development, from clinical trials to registration.

CliniCore is part of the Synvia software family. Each platform covers a stage of development, from clinical trials to registration.

Synvia TrialCore

Connects data, processes, and teams throughout the entire clinical study lifecycle, bringing together eCRF, CTMS, eTMF, and ePRO into a single integrated platform.

Synvia TrialCore

Connects data, processes, and teams throughout the entire clinical study lifecycle, bringing together eCRF, CTMS, eTMF, and ePRO into a single integrated platform.

Synvia RegCore

Leads the drug's path to registration, from study reports to submissions for ANVISA, FDA, EMA, and other international agencies.

Synvia RegCore

Leads the drug's path to registration, from study reports to submissions for ANVISA, FDA, EMA, and other international agencies.

Waiting list

Your center among the top

O CliniCore está em fase final de lançamento.

O acesso é liberado por etapas e os centros inscritos entram primeiro, com onboarding assistido.

Priority access in order of registration

Priority access in order of registration

Onboarding assisted by the Synvia team

Onboarding assisted by the Synvia team

Guaranteed launch condition for your center

Guaranteed launch condition for your center

Join the waitlist

Join the waitlist

Your data will only be used to communicate the launch, in accordance with the LGPD.

Your data will only be used to communicate the launch, in accordance with the LGPD.

Your data will only be used to communicate the launch, in accordance with the LGPD.

Waiting list

Your center among the top

O CliniCore está em fase final de lançamento.

O acesso é liberado por etapas e os centros inscritos entram primeiro, com onboarding assistido.

Priority access in order of registration

Onboarding assisted by the Synvia team

Guaranteed launch condition for your center

Join the waitlist

Your data will only be used to communicate the launch, in accordance with the LGPD.