Why MediRama
Why MediRama
With years of experience in global clinical trials and oncology drug development, MediRama offers an expert
team skilled in navigating complex regulatory landscapes. The team’s experience includes the FDA’s
Accelerated Approval, Fast Track, Breakthrough Therapy, and Priority Review pathways,
enabling faster, more efficient development timelines.
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Unmatched Expertise in
Clinical Development
and Regulatory Strategy -
Comprehensive and Tailored
Solutions -
Advanced
Operational Models -
Strong Global Network
and Regional Expertise -
Proven Track Record in Oncology
Drug Development -
Commitment to
Innovation and Quality
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364No of Clinical Projects that MediRama Staffs have managed
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40No of consulting projects done or currently ongoing by MediRama
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101Total years of Clinical Experience by
MediRama Staffs (MDs & RNs) -
33Total years of
RA Experience by
MediRama Staffs -
30No of Multinational Pharmaceutical Company experiences by MediRama employees
-
37Total years of Commercial Experience by MediRama
Staffs -
247Total years of MediRama Staffs’ seniorities in Biotech/Pharma industry and Govm
