Welcome to MonTox Services, LLC
At MonTox Services, LLC, we specialize in providing expert scientific advice and operational support tailored to the pharmaceutical and biotechnology industries. Our dedicated team is committed to guiding you through the complexities of nonclinical drug development, ensuring your projects are positioned for success. Partner with us to navigate the path from concept to market with confidence and precision.
Features
Expert Guidance
Our team of seasoned professionals offers tailored scientific advice, ensuring your drug development process is efficient and compliant with industry standards.
Operational Support
We provide comprehensive operational support, from project management to regulatory strategy, helping you navigate the complexities of nonclinical drug development.
Customized Solutions
At MonTox Services, we understand that every project is unique. We deliver customized solutions that align with your specific goals and timelines.
Collaborative Approach
We believe in a collaborative approach, working closely with your team to foster innovation and drive successful outcomes in your drug development journey.
About MonTox Services, LLC.
At MonTox Services, LLC., we specialize in providing expert scientific advice and operational support tailored to the unique needs of the pharmaceutical and biotechnology industries. Our team of seasoned professionals is dedicated to guiding clients through the complexities of nonclinical drug development, ensuring that every project is approached with precision and a commitment to excellence. With a focus on innovation and collaboration, we empower our partners to navigate the drug development landscape effectively, ultimately bringing life-changing therapies to market.
Stephene Ford has over 29 years of experience working in the pharmaceutical industry, with specific knowledge in the development of vaccine, infectious disease and biologic programs (including up to BSL 2/3). She spent 17 years as a Study Director at CRL (Reno, NV and Mattawan, MI) and was responsible for the planning and conduct of nonclinical studies in accordance with applicable regulatory guidelines and contemporary scientific practice.
Professionals
Stephene Ford
Owner
Johnny Carter
Regulatory Affairs Specialist
Lisa Brown
Clinical Operations Manager
Kimberly Baker
Project Coordinator
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