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.

Two people in lab coats collaborate in an office setting. One is seated and pointing at a computer screen displaying medical images, while the other stands nearby holding a tablet. Large windows reveal a view of greenery outside, creating a bright and professional environment.
Two people in lab coats collaborate in an office setting. One is seated and pointing at a computer screen displaying medical images, while the other stands nearby holding a tablet. Large windows reveal a view of greenery outside, creating a bright and professional environment.

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.

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M4 full logo

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