Pharmacovigilance & Medical Affairs
Integrated safety monitoring and medical-scientific support
Safety management is a critical element throughout
clinical development. Our involvement in pharmacovigilance, medical affairs, and support for Independent Data Monitoring Committees (DSMB) ensures a continuous and rigorous assessment of the risk-benefit relationship, supporting clinical, ethical, and regulatory decisions based on scientific evidence.
Pharmacovigilance
We offer comprehensive pharmacovigilance services for clinical studies, ensuring the identification, evaluation, monitoring, and proper communication of adverse events, in compliance with local and international regulations.
Medical Affairs
Our Medical Affairs team acts as a link between science, clinical practice, and strategy, providing medical-scientific support for the safe and consistent conduct of clinical trials.
Synvia
Why choose Synvia
More than two decades of experience across the entire drug research and registration chain.
We integrate clinical research, laboratory analyses, and technology to meet the demands of the pharmaceutical industry with quality and global compliance.
