DUE DILIGENCE PROJECTS, FIRST-IN-HUMAN/FIRST-IN-PLATFORM CLINICAL TRIALS DESIGN AND CONDUCT, FRACTIONAL CMO SUPPORT
About M Consulting
We believe that your early phase clinical trials should be tailored to your specific new molecular entity. We fully assess the unique features of your compound, strategic development plan, and resource allocation to determine the clinical trial design that provides the safest, quickest, and most informative study.


Our Expertise
We bring experience from investigator and sponsor, clinical pharmacology and medical, small molecule, gene editing, and cellular therapy perspectives. We are uniquely qualified to facilitate first-in-human and first-in-platform development projects in oncology and rare diseases.


