Jordana A.

I am a scientific consultant specializing in toxicology, safety assessment, and preclinical research. I hold a PhD in Pharmaceutical Sciences and have over six years of research experience, supporting pharmaceutical, cosmetic, and biotechnology companies in translating complex scientific data into regulatory compliance strategies. 🎯My expertise lies in nonclinical study design with a focus on in vitro toxicology (OECD/ISO/NAMs), biocompatibility assessment (ISO 10993), and the development of regulatory documentation, such as: - Nonclinical sections for CTDs (IMPD, IND, IB) - Safety reports for cosmetics (PIF, CPSR) - Biocompatibility dossiers for medical devices - Technical summaries and scientific white papers for investors and partners I have hands-on experience with advanced cellular models, including 3D tissue models, organ-on-a-chip systems, and microphysiological platforms, particularly for cutaneous, ocular, and respiratory applications. Working with biotechnology startups, contract research organizations (CROs), and academic laboratories, always connecting innovation and application. 💼 Professional Highlights: - Toxicology consultant on more than 3 international regulatory projects - Developer of in vitro POC models for skin and retina using stem cells and biomaterials - Collaborator on funding proposals and market/technology prospecting for NAMs - Trained by TissUse GmbH (Berlin) and Epithelix (Geneva) in MPS and inhalation toxicology - Scientific analyst at Prescouter, providing insights for clients such as Abbott, Roche, BD, Zoetis, and Elanco Whether you're looking for support with a nonclinical development strategy, technical writing, or toxicological risk assessment, I'm here to help you drive your innovation forward with confidence and regulatory clarity. Let's work together to bring safe, effective, and innovative products to market!