Clinical studies center specializing in phases I to IV
Our multisite structure allows for conducting clinical trials with safety, precision, and predictability. We operate with international quality standards, ensuring consistent deliveries for the global pharmaceutical industry.
research participants
20,000 m² of complete infrastructure, ready for bioequivalence studies
Complete installations that meet end-to-end projects, ensuring maximum efficiency and agility.
Integrated and multidisciplinary coordination
The support areas of Synvia work in coordination with the clinical teams, ensuring that each study is conducted with technical precision, regulatory compliance, and operational efficiency.
Excellence in quality, safety, and regulatory-scientific compliance
Global Regulatory Compliance
Full compliance with Good Clinical Practices (ICH E6 R2), ANVISA, and international standards, ensuring auditable and traceable studies.
Essential documentation for audits and submissions:
Extensive experience in multiple therapeutic areas
Our studies cover various medical specialties and specialized technical teams.
Pharma Solutions
Integrated solutions for the pharmaceutical industry
From clinical research to laboratory analyses and regulatory studies, our Pharma solutions connect all the necessary steps for the development, validation, and registration of medications.
Join the Medical Referring Program
The network that connects specialists to clinical research with ethics, safety, and purpose.
Contact
Talk to our experts
Discover how Synvia can support your studies, analyses, and projects.
Operational Procedure List
Standard Operating Procedures (SOPs)