The best solution for your projects.

We customize our services to your needs, being able to provide solutions to specific outsourcing activities, from regulatory strategies to statistical analysis. 

Project Management

Driving clinical excellence with strategic problem solving.

Strong, communicative, detail-oriented project team, with a robust problem-solving mindset, ensures clinical trial deliverables and timelines are met.

Synvia CRO 

is a Contract Research Organization with over 20 years of experience and more than 200 satisfied pharmaceutical clients around the world. 

We offer a comprehensive range of services, from phase I to IV clinical trials in a full-service model to specialized support in regulatory, scientific and clinical operations. 

Our modular approach provides customized solutions for specific needs always committed to offer quality and excellence to our clients.  

Regulatory Affairs

Technical-regulatory alignment.

We will find the best regulatory strategy for your product, identifying the appropriate pathway within the current local environment and the leading regulatory authorities.

Medical Writing

  • Clinical study protocol 
  • Informed Consent Form (ICF) 
  • Clinical Study Report (CSR) 
  • Investigator’s brochure 
  • Patient questionnaire 
  • Scientific publications 
  • Safety and efficacy reports/rationale 

Scientific documents of different types 

Medical writers are ready to assist your company in preparing scientific documents, including regulatory and research-related materials. With expertise in science, research, and current guidelines, we ensure the information is presented at the right level for your needs. 

Biostatistics

  •  Endpoint development for study design in cooperation with medical writing teams 
  • Sample size calculations and randomization schemes 
  • Statistical analysis 
  • Statistical Analysis Plan (SAP) development 
  • Technical meetings with regulatory agencies 

High-complexity diagnostic analysis 

Analytical support for clinical trials, offering a range of solutions from targeted to full-service, with a focus on customization and development. ​

Why conduct clinical trials in Brazil?

Brazil offers a diverse population of 220 million, a high-quality network of hospitals, and a well-respected regulatory agency, ANVISA. The Brazilian pharmaceutical market is one of the largest in the world and maintains robust annual growth.  

Synvia CRO supports companies that want to access this Market as well as companies that are just looking for the most cost-effective alternative for clinical trials worldwide.  

Our international reach and local expertise ensure seamless and effective solutions for our sponsors. 

State-of-the-art services

We provide comprehensive support for the importation of controlled and non-controlled materials in clinical trials. We handle every step — from currency exchange and SWIFT processing to final reporting — all to provide the most cost-effective solutions for our clients.

Logistical and regulatory management

Coordination of transport, flights, and material storage  

Issuance of authorizations and reporting to ANVISA and the Federal Revenue Service 

Cost analysis and negotiation for better pricing  

Contact us:

Fill out the form, if you are interested to be a partner.

Rua Mário Giordano, 146 - Jardim América, Paulínia - SP, 13140-614 - Brazil

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Clinical Monitoring

  • Site identification, qualification, and selection 
  • Regulatory document preparation and collection 
  • General contract negotiation 
  • Investigator meeting planning and presentation 
  • Handling of SAE 
  • Site personnel training 
  • Remote and on-site monitoring 
  • Investigational product and materials accountability 
  • Closeout visits 

Data quality and integrity.

Highly qualified monitoring professionals, certified in advanced tools, ensure the integrity and quality of data collected during the study.  

Central Laboratory

  • Manufacturing and distribution of laboratory kits 
  • Management of the entire logistics chain, prioritizing the safety, speed, and integrity of the samples 
  • Over 4,000 tests in our portfolio 
  • 400+ validated methods for different drug formulations 
  • 100,000+ samples processed per month  
  • 30+ LC-MS/MS systems  

State-of-the-art services

Personalized Experience 

We provide the personalized and boutique service you would expect from a smaller CRO while being backed by a large, consolidated group. 

Your full-service CRO in Brazil.

  • Ensure compliance with protocols, guidelines, legislation, and SOPs
  • Plan, initiate, and manage clinical projects
  • Risk assessment and mitigation
  • Primary contact for sponsors and project teams
  • Develop TMF/eTMF and research documents
  • Resource management
  • Contract negotiation
  • Financial control
  • Regulatory strategies 
  • Agency interactions 
  • Regulatory feasibility 
  • Gap analysis/ Due diligence 
  • Elaboration of dossiers 
  • Regulatory lifecycle management 

One of the main pillars of scientific research

Biostatistics has become increasingly important and relevant in recent years. Our team of specialists is ready to meet your needs, providing comprehensive support at every stage.  

End-to-End Solutions 

Streamline your operations by outsourcing all your needs to a single company, ensuring seamless and effective integration with one point of contact.  

Competitive Pricing 

Our extensive knowledge of the clinical trials landscape in Brazil enables us to deliver top-quality services at competitive prices.