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About us

Harmonized Studies

About us

Harmonized Studies

About us

Harmonized Studies

About us

Harmonized Studies

Globally harmonized studies with regulatory excellence

A single protocol, multiple submissions

Our harmonized studies follow standardized international guidelines, allowing a single study to be used for regulatory submissions in different countries. We reduce time and costs while maintaining full compliance and scientific integrity.

Harmonized protocols accepted in multiple regions

Harmonized protocols accepted in multiple regions

Harmonized protocols accepted in multiple regions

Harmonized protocols accepted in multiple regions

Documentation in Portuguese, English, and Spanish

Documentation in Portuguese, English, and Spanish

Documentation in Portuguese, English, and Spanish

Documentation in Portuguese, English, and Spanish

Integrated logistics and regulatory management

Integrated logistics and regulatory management

Integrated logistics and regulatory management

Integrated logistics and regulatory management

Compliance proven with EMA and FDA

Compliance proven with EMA and FDA

Compliance proven with EMA and FDA

Compliance proven with EMA and FDA

A single partner, complete scientific infrastructure

Based in Brazil, Synvia integrates clinical, analytical, and regulatory expertise to deliver harmonized studies ready for international submission. With 20 years of experience, over 1,600 studies conducted, and the largest analytical facility in Latin America in LC-MS/MS.

Bioequivalence and PK/PD studies

Bioequivalence and PK/PD studies

Bioequivalence and PK/PD studies

Bioequivalence and PK/PD studies

Pharmaceutical equivalence and in vitro studies

Pharmaceutical equivalence and in vitro studies

Pharmaceutical equivalence and in vitro studies

Pharmaceutical equivalence and in vitro studies

Phase I to IV clinical trials

Phase I to IV clinical trials

Phase I to IV clinical trials

Phase I to IV clinical trials

Biosimilars and others

Biosimilars and others

Biosimilars and others

Biosimilars and others

Our schedule, your differential

Our numbers

Collaborators

+700

Collaborators

+700

Collaborators

+700

Collaborators

+700

Clinical studies conducted

+0thousand

Clinical studies conducted

+0thousand

Clinical studies conducted

+0thousand

Clinical studies conducted

+0thousand

Research participants

+0thousand

Research participants

+0thousand

Research participants

+0thousand

Research participants

+0thousand

People in database

+100thousand

People in database

+100thousand

People in database

+100thousand

People in database

+100thousand

Why choose Synvia

Why choose Synvia

Experience, compliance, and scientific accuracy

Experience, compliance, and scientific accuracy

Synvia has a history of success in studies submitted and approved by different regulatory authorities.

Our operational model follows global quality standards, ensuring complete traceability and trilingual documentation.

Synvia has a history of success in studies submitted and approved by different regulatory authorities.

Our operational model follows global quality standards, ensuring complete traceability and trilingual documentation.

Validated infrastructure and global compliance

Our facilities meet international quality and safety standards, ensuring the credibility of every result delivered.

ANVISA
ANVISA
ANVISA
ANVISA
EMA
EMA
EMA
EMA
FDA
FDA
FDA
FDA
GCC
GCC
GCC
GCC

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.