Mesa offers a unique blend of highly specialized experiences and skills vital to the drug development process. Our team has extensive experience working on successful auto-injector programs for the U.S. government, allied governments, and for civilian use, gaining expertise that is easily transferable to other methods of drug delivery.
When you work with us, you will benefit from access to numerous experienced field professionals who know the drug development process better than their competitors. Familiarize yourself with the services that will put your drug development project on the best path forward.
Clinical studies are paramount in the development process of a drug, and we pull from our decades of combined experience to make sure yours runs smoothly. We have experience working across Phase 1 to 4 clinical trials and assign monitors based on your trial’s needs.
We have the expertise to evaluate your active pharmaceutical ingredient (API), characterize it, and design a formulation that meets its associated medical needs. Every formulation is developed and tested appropriately through commercial scales.
Our team has decades of experience in the design and development of CMC drug delivery systems. We stand ready to assist in all aspects of your drug delivery project—from design and drug development to human factor and reliability studies.
We can generate experimental protocols for both clinical and preclinical studies, provide oversight of the experiments, help in the determination of the experimental results and generate all required reports to both Sponsors and the FDA.
We have been involved in conducting pre-clinical studies for over five decades. We can help generate experimental protocols, provide oversight of the experiments, help in the interpretation of the results and generate final reports so you can get your drug to market faster.
Our project management services drive execution, track progress, and capture performance measures through work breakdown structures, coping and planning, addressing baseline milestones in the drug development process, and more.
Before you’re ready to have your drug evaluated by regulatory bodies, there are several steps that should be taken to ensure it will pass. Through everything from shelf-life studies to drug impurity identification, we’ll run the tests that allow you to identify areas for improvement.
Our services focus on bridging the gap between you and the regulatory bodies that provide approval. When you partner with us, we will make sure your drug meets all legal and safety standards throughout the development process.
Comprehensive site management and monitoring services are required when developing any drug. These services include site identification, staff training, risk-based monitoring, safety management, and more.
A Veteran Owned Small Business
Our mission is to work with you to develop and commercialize novel pharmaceutical products. Through this collaboration, we can deliver life-changing therapies that fill vital unmet needs. As a veteran-owned business, we understand the necessity to protect the life and health of everyone who needs assistance.
What’s going on at Mesa and in the pharmaceutical world at large? Explore this section to find out!
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