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Software

Synvia eCRF

Software

Synvia eCRF

Software

Synvia eCRF

Software

Synvia eCRF

Synvia eCRF: national technology, global standard

Quality and safety

Clinical data management with cutting-edge technology and regulatory compliance

The Synvia eCRF digitizes and centralizes the collection of clinical data throughout the study — from field filling to the final database — ensuring information integrity, complete traceability, and operational efficiency, in full compliance with national and international regulatory requirements (ANVISA, ICH-GCP, EMA, and FDA).

ANVISA
ANVISA
ANVISA
ANVISA
FDA 21 CRF PART 1
FDA 21 CRF PART 1
FDA 21 CRF PART 1
FDA 21 CRF PART 1
EMA
EMA
EMA
EMA
I
I
I
I

High-performance solution that brings more precision, agility, and innovation to clinical studies.

Enhanced efficiency:

Collection and analysis of data in a simplified way

Enhanced efficiency:

Collection and analysis of data in a simplified way

Enhanced efficiency:

Collection and analysis of data in a simplified way

Enhanced efficiency:

Collection and analysis of data in a simplified way

Optimized cost:

Solution with optimized cost for the Brazilian market

Optimized cost:

Solution with optimized cost for the Brazilian market

Optimized cost:

Solution with optimized cost for the Brazilian market

Optimized cost:

Solution with optimized cost for the Brazilian market

Agile decisions:

Data updated in real time

Agile decisions:

Data updated in real time

Agile decisions:

Data updated in real time

Agile decisions:

Data updated in real time

Greater accuracy:

Automation and validations minimize human errors

Greater accuracy:

Automation and validations minimize human errors

Greater accuracy:

Automation and validations minimize human errors

Greater accuracy:

Automation and validations minimize human errors

Advanced technology:

Application of Artificial Intelligence and robust integrations

Advanced technology:

Application of Artificial Intelligence and robust integrations

Advanced technology:

Application of Artificial Intelligence and robust integrations

Advanced technology:

Application of Artificial Intelligence and robust integrations

Agile and efficient support:

Quick responses and improvements implemented promptly.

Agile and efficient support:

Quick responses and improvements implemented promptly.

Agile and efficient support:

Quick responses and improvements implemented promptly.

Agile and efficient support:

Quick responses and improvements implemented promptly.

Standard Modules

Main features

Information Security

Advanced encryption, access control, and international regulatory compliance

Information Security

Advanced encryption, access control, and international regulatory compliance

Information Security

Advanced encryption, access control, and international regulatory compliance

Anonymization of participants

Inclusion of participants in a secure and anonymous way, ensuring data protection.

Anonymization of participants

Inclusion of participants in a secure and anonymous way, ensuring data protection.

Anonymization of participants

Inclusion of participants in a secure and anonymous way, ensuring data protection.

Queries and Data

Efficient query management and data consistency assurance

Queries and Data

Efficient query management and data consistency assurance

Queries and Data

Efficient query management and data consistency assurance

Forms Status

Detailed tracking of form completion

Forms Status

Detailed tracking of form completion

Forms Status

Detailed tracking of form completion

Real Time Reports

Detailed reports available in real-time for monitoring

Real Time Reports

Detailed reports available in real-time for monitoring

Real Time Reports

Detailed reports available in real-time for monitoring

Electronic Forms

Guaranteed secure, accurate, and standardized data collection

Electronic Forms

Guaranteed secure, accurate, and standardized data collection

Electronic Forms

Guaranteed secure, accurate, and standardized data collection

Source Data Verification (SDV)

Resource for managing the monitoring activities (SDV) of the study

Source Data Verification (SDV)

Resource for managing the monitoring activities (SDV) of the study

Source Data Verification (SDV)

Resource for managing the monitoring activities (SDV) of the study

Participant Status

Inclusion of participants in a secure and anonymous way, ensuring data protection.

Participant Status

Inclusion of participants in a secure and anonymous way, ensuring data protection.

Participant Status

Inclusion of participants in a secure and anonymous way, ensuring data protection.

User Management

Strict control of user access and their permissions (roles) within the eCRF

User Management

Strict control of user access and their permissions (roles) within the eCRF

User Management

Strict control of user access and their permissions (roles) within the eCRF

Optional Modules

Add more features to your system

The platform that stands out in the market and drives clinical studies

Regulatory Compliance

Regulatory Compliance

Investment

Investment

Performance

Performance

Usability

Usability

Auditability

Auditability

Flexibility and scalability

Flexibility and scalability

Implementation

Implementation

Technical support & Improvements

Technical support & Improvements

Synvia eCRF

National platform,
global standard

Fully complies with national and international standards

Fully complies with national and international standards

Fully complies with national and international standards

Fully complies with national and international standards

National reality

Investment compatible with the national reality

National reality

National reality

Optimized for exceptional performance

Optimized for exceptional performance

Optimized for exceptional performance

Optimized for exceptional performance

Friendly and intuitive interface

Friendly and intuitive interface

Friendly and intuitive interface

Friendly and intuitive interface

Controlled, tracked, and auditable record of operations

Controlled, tracked, and auditable record of operations

Controlled, tracked, and auditable record of operations

Controlled, tracked, and auditable record of operations

Highly adaptable to various and complex studies

Highly adaptable to various and complex studies

Highly adaptable to various and complex studies

Highly adaptable to various and complex studies

Quick implementation with personalized training

Quick implementation with personalized training

Quick implementation with personalized training

Quick implementation with personalized training

Agile and personalized

Agile and personalized support

Agile and personalized

Agile and personalized support

Other platforms

They may not meet all regulatory requirements

They may not meet all regulatory requirements

They may not meet all regulatory requirements

Insecurity regarding exchange rate variation

Insecurity regarding exchange rate variation

Insecurity regarding exchange rate variation

Low performance

Low performance

Low performance

Complex interfaces

Complex interfaces

Complex interfaces

Limited records

Limited records

Limited records

Restricted options

Restricted options

Restricted options

Extensive training

Extensive training

Extensive training

Bureaucratic processes and little flexibility

Bureaucratic processes and little flexibility

Bureaucratic processes and little flexibility

Synvia ePRO

Connect participants to clinical studies in real time – simple, safe, and regulatory compliant.

Native integration with Synvia eCRF ensuring consistency, traceability, and elimination of rework.

Native integration with Synvia eCRF ensuring consistency, traceability, and elimination of rework.

Native integration with Synvia eCRF ensuring consistency, traceability, and elimination of rework.

Native integration with Synvia eCRF ensuring consistency, traceability, and elimination of rework.

Intuitive application for the research participant, with smart reminders and notifications.

Intuitive application for the research participant, with smart reminders and notifications.

Intuitive application for the research participant, with smart reminders and notifications.

Intuitive application for the research participant, with smart reminders and notifications.

Remote and centralized monitoring for more agile and assertive decisions.

Remote and centralized monitoring for more agile and assertive decisions.

Remote and centralized monitoring for more agile and assertive decisions.

Remote and centralized monitoring for more agile and assertive decisions.

Data Management

Complete clinical data management service:

Development planning for eCRF

Development planning for eCRF

Development planning for eCRF

Development planning for eCRF

Guarantee of standardized and efficient processes that comply with regulatory requirements

Guarantee of standardized and efficient processes that comply with regulatory requirements

Guarantee of standardized and efficient processes that comply with regulatory requirements

Guarantee of standardized and efficient processes that comply with regulatory requirements

Real-time, consistent, secure, and traceable data acquisition

Real-time, consistent, secure, and traceable data acquisition

Real-time, consistent, secure, and traceable data acquisition

Real-time, consistent, secure, and traceable data acquisition

Synvia LIS

The Synvia LIS automates the complete laboratory workflow, ensuring traceability, efficiency, and proven compliance, recognized by international certifications.

Synvia LIS

The Synvia LIS automates the complete laboratory workflow, ensuring traceability, efficiency, and proven compliance, recognized by international certifications.

Synvia LIS

The Synvia LIS automates the complete laboratory workflow, ensuring traceability, efficiency, and proven compliance, recognized by international certifications.

Synvia LIS

The Synvia LIS automates the complete laboratory workflow, ensuring traceability, efficiency, and proven compliance, recognized by international certifications.

Synvia CTMS

Electronic data collection platform reported directly by participants, ideal for sponsors and research centers.

Synvia CTMS

Electronic data collection platform reported directly by participants, ideal for sponsors and research centers.

Synvia CTMS

Electronic data collection platform reported directly by participants, ideal for sponsors and research centers.

Synvia CTMS

Electronic data collection platform reported directly by participants, ideal for sponsors and research centers.

Synvia eTMF

Electronic management platform for the Trial Master File, with organization, traceability, and control of regulatory document versions, ideal for sponsors and research centers.

Synvia eTMF

Electronic management platform for the Trial Master File, with organization, traceability, and control of regulatory document versions, ideal for sponsors and research centers.

Synvia eTMF

Electronic management platform for the Trial Master File, with organization, traceability, and control of regulatory document versions, ideal for sponsors and research centers.

Synvia eTMF

Electronic management platform for the Trial Master File, with organization, traceability, and control of regulatory document versions, ideal for sponsors and research centers.

Contact

Talk to our experts

Discover how Synvia can support your studies, analyses, and projects.

Contact

Talk to our experts

Discover how Synvia can support your studies, analyses, and projects.