ABOUT US

Our Mission

Altus Trece is a highly specialized consulting firm that excels at designing regulatory strategies and managing scientific research in close collaboration with health authorities. Our service portfolio covers a wide range of areas, from project design to the generation of medical device documentation. We are distinguished by our rigorous focus on continuous improvement of manufacturing processes and strict compliance with regulatory standards.

Our commitment is based on excellence, transparency, and adaptability to our clients' needs, ensuring the acquisition of registrations and licenses, the development of protocols supported by data and best practices, as well as the implementation of quality systems aligned with international standards.

OUR TEAM

Team of Experts

Our team of consultants is comprised of experienced researchers with a solid scientific background and a proven track record of results. Their specialized knowledge and collaborative approach allow us to successfully navigate today's complex regulatory landscape, ensuring the quality and effectiveness of our services.

Yarabey Encalada

CEO

Professional with over a decade of experience in the pharmaceutical industry, excelling in the areas of manufacturing, research and development, and formulation, as well as process validation (IQ/OQ/PQ) and quality assurance.
Her experience includes a specialized focus on regulatory affairs for foreign companies operating in Mexico, supporting the acquisition of health registrations, import permits, and compliance with NOM/ICH regulations through close collaboration with COFEPRIS and other health authorities.
She has a solid academic background in chemistry (MS) and biology (BS) from renowned institutions (Miami University and the Autonomous University of Guadalajara). She is recognized for her ability to design and optimize processes, manage regulatory filings, and deliver tailored solutions that balance delivery times, costs, and quality.

His leadership is interdisciplinary, with a knack for communicating with international authorities and clients, and is characterized by a commitment to excellence and innovation to ensure compliance with GMP and Mexican regulatory frameworks.

Anna Santos

Project Director

Professional specialized in comprehensive project management within the pharmaceutical, biotechnology, and medical device sectors, with extensive experience coordinating regulatory and operational processes in accordance with Mexican regulations.
Throughout his career, he has led projects focused on the introduction, registration, transfer, and monitoring of pharmaceutical products and medical devices, ensuring regulatory compliance and emphasizing the optimization of time and resources.
Its approach combines a strategic vision with precise technical execution, ensuring document traceability, risk assessment, and alignment with national and international standards.
She has solid skills in planning, monitoring, and controlling multidisciplinary projects, as well as in integrating technical, regulatory, and commercial teams. Her analytical skills and effective communication skills have allowed her to serve as a key liaison between laboratories, health authorities, consulting firms, and strategic partners, promoting high-impact projects in the Mexican and Latin American pharmaceutical markets.

He stands out for his results-oriented leadership, critical thinking, and commitment to innovation, transparency, and quality at every stage of each project's lifecycle.

Yarabey Encalada

CEO

Professional with over a decade of experience in the pharmaceutical industry, excelling in the areas of manufacturing, research and development, and formulation, as well as process validation (IQ/OQ/PQ) and quality assurance.
Her experience includes a specialized focus on regulatory affairs for foreign companies operating in Mexico, supporting the acquisition of health registrations, import permits, and compliance with NOM/ICH regulations through close collaboration with COFEPRIS and other health authorities.
She has a solid academic background in chemistry (MS) and biology (BS) from renowned institutions (Miami University and the Autonomous University of Guadalajara). She is recognized for her ability to design and optimize processes, manage regulatory filings, and deliver tailored solutions that balance delivery times, costs, and quality.

His leadership is interdisciplinary, with a knack for communicating with international authorities and clients, and is characterized by a commitment to excellence and innovation to ensure compliance with GMP and Mexican regulatory frameworks.

CUSTOMERS

Nuestros Socios

We have had the privilege of collaborating with a wide range of clients, from medical device manufacturers to pharmaceutical distributors. Our ability to offer tailored solutions and our focus on quality and regulatory compliance have allowed us to establish strong and lasting relationships with our business partners.

Our clients trust us to provide comprehensive solutions tailored to their specific needs and focused on achieving tangible and sustainable results. Their success is our success, and we are proud to be part of their journey toward excellence.