Mariah Ultramari Email & Phone Number

São Paulo, São Paulo, Brazil

With more than 1000 reports approved by “ANVISA” in my career (“National Health Surveillance Agency”), Spektra was born based on our trust to build up solid and ethical partnerships worldwide towards a unique purpose: to safely serve the society.A consultancy company focused on Toxicology which is always aiming to understand its impacts from the Regulatory requirements until the Practical solutions. Global partners allow us to anticipate trends and work with the best tools available in the industry, whereas our local and regional partners constitute our strong networking with the best professionals in the industry for serving our customers. The opportunity to work nearly 6 years in the Pharmaceutical Industry, right after completing my Ph.D. in Toxicology was a life-change experience for which I am very grateful. However, I had the feeling I could contribute more if I took the chance to establish my own company in order to expand the horizons of my dedication. Since early 2019 I started this journey which has been challenging but full of great achievements.

Califórnia, Estados Unidos

“Fusion QbD” Solutions - Representative and Technical Support for Brazil and LATAM.Fusion QbD Software Platform incorporates expert-system guided statistical Design of Experiments (DOE) and multivariate data analysis/modeling technologies within a Quality by Design (QbD) framework. Tailored modules are designed for targeted applications in Analytical, Formulation, and Chemical and Process R&D laboratories within the Pharmaceutical, Biotechnology, and Chemical industries.We are honored to represent this top of class technology to support our customers in Latin America.

Brazil

FreeThink is the scientific expert in stability, committed to developing phase-appropriate stability-indicating methods and applying them to your project. We lead the industry in accelerated processes for modeling product shelf-life, obtaining results in just a few weeks using the ASAPprime® stability software we developed. Our team also excels at longer-term traditional studies, such as those based on the ICH guidelines, and cGMP studies that meet all criteria for regulatory filings. In our state-of-the-art labs, stability studies range from quick evaluations to the most challenging in-depth problem solving. As a result, we are adept at helping customers find appropriate, cost-effective solutions to their stability challenges, including physical changes of active forms, formulations, packaging and storage conditions.

São Paulo, Brasil

- Opportunity to apply in practice, all theory learned during the Doctorate - Team Leader, responsible for impurities’ assessment (analytical development and toxicological evaluation) - Responsible for establishing a BRL 11 Mln laboratory within one of the biggest industries in the country. - People management: leader of a team with 8 scientists - Networking: Establishment of a good relationship with Regulators and Colleagues from the industry- ANVISA (“National Health Surveillance Agency”): Responsible for all interactions with the Brazilian Regulator, regarding impurities and toxicology

São Paulo E Região, Brasil

Doutorado desenvolvido em estudos de degradação forçada, desenvolvimento de métodos indicativos de estabilidade e avaliação da toxicidade de produtos de degradação de medicamentos

Doctor Of Philosophy (Phd), Toxicologia E Análises Toxicológicas

Activities and Societies: Representante discente (2012/2013) do Programa de Pós Graduação de Toxicologia e Análises Toxicológicas.

Farmacêutica, Farmácia, Graduação