Specialized Solutions for CROs and the Biotechnology Industry
Our Services
Conducting clinical trials - laboratory (Phases I–IV) focused on pharmaceutical studies.
Specialized regulatory consulting – ANVISA, covering in vitro medical devices and pharmaceutical projects.
Recruitment and management of biological samples, with a diverse network of partner centers and laboratories.
Data analysis and advanced biostatistics , ensuring methodological robustness and accurate scientific interpretation.
Medical writing and scientific communication, including the preparation of technical reports, publications, and regulatory submissions.
Main Differentiators
Fast and predictable regulatory approval
Facilitated access for diverse patient populations.
Efficient cost and resource management
Digital innovation applied to clinical research
Strict compliance with global standards
Why choose Scientific Base?
Fast approval of documentation by ANVISA, reflecting technical excellence and regulatory alignment of our dossiers and protocols.
Team with extensive experience in national and international regulation (ANVISA, FDA, EMA).
Integrated solutions, ranging from protocol design to post-market follow-up.
Proven track record of success with leaders in the pharmaceutical, biotechnology, and CRO industries.