Medical Writing & Scientific Documentation

Medical Writing

Medical Writing & Scientific Documentation

Especialista da Synvia elaborando documentos científicos e regulatórios para estudos clínicos

Scientific documents across multiple disciplines

Preparation of clinical and regulatory documents, clinical development (protocols, CSR, IB, informed consent, manuscripts) with scientific clarity and international standardization.

Medical Writers

With a team of medical writers with solid scientific expertise in clinical research and a deep understanding of current guidelines, we ensure that the information is presented with accuracy, clarity, and a robust technical level.

Clinical study protocol

Clinical study protocol

Informed Consent Form (ICF)

Informed Consent Form (ICF)

Clinical Study Report (CSR)

Clinical Study Report (CSR)

Investigator's Brochure (IB)

Investigator's Brochure (IB)

Questionnaires for patients

Questionnaires for patients

Scientific publications

Scientific publications

Reports and rationale for safety and efficacy

Reports and rationale for safety and efficacy

Medical writer da Synvia especializada em elaboração de protocolos clínicos e relatórios científicos

Synvia

Why choose Synvia

More than two decades of acting throughout the entire chain

of research and drug registration.


We integrate clinical research, laboratory analyses, and technology to meet the demands of the pharmaceutical industry with quality and global compliance.

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.