Alexandra Reis, PhD
CSO — Chief Scientific Officer
PhD in Infectious Diseases from USP and specialist in Tropical Diseases. With experience in translational research, she leads the scientific strategy and project management at Base Científica.
Who we are
A research center with a specialized laboratory for your innovation.
We were built to serve pharma and diagnostics with the rigor of a central lab and the agility of a small dedicated team.
Base Científica acts as the advanced scientific engineering arm of companies that require complex analytical assays, regulatory validation to international standards and unequivocal authentication of biological raw materials.
We are not a commodity lab. Each project is led by a PhD specialist, executed under strict NDA and designed from the product's risk profile.
We serve clients in Brazil, Europe, the United States and Asia, with bilingual documentation and ANVISA, FDA, EMA and ICH compliance.
Trust
Chosen by those who demand scientific depth.
Clients, academic partners and certifications that sustain our standard.
Selected clients
Partners & certifications
PALC — SBPC/ML
DNA USP
Karolinska Institute
Biominas Brasil
Technical leadership
A PhD core accountable for the scope, from design to dossier.
Every project is led by a senior specialist — close to the bench and to the scientific decision.
Érika Machado, PhD
Director of Scientific Development
PhD in Immunology from USP with more than 10 years of experience in basic and applied research. She works on the validation of immunological therapies and diagnostics, with publications in high-impact scientific journals.
Robson Amaral, PhD
Director of Cell Culture Technology
PhD in Pharmaceutical Sciences from USP, with additional training in biotechnology at Newcastle University (UK) and oncology at the University of California (USA). He has 14 years of experience in cell culture, specialising in 3D cultures, tumour organoids and preclinical testing for personalised oncology.
Scientific rigor
Every deliverable is reviewed by a PhD committee. No shortcuts.
Global compliance
ANVISA, FDA, EMA, ICH, ISO 17025 and GLP — from first draft to final dossier.
Weekly cadence
Transparent communication, objective metrics and real visibility over progress.