Gliese 623b

Gliese623B provides consultant services in the areas of pre-clinical medical device validation support for 510K premarket notification submissions with the FDA. We also provide drug discovery solutions and manufacture support, study design & protocol development, pre-clinical method validation, R&D outsourcing, SOP authorship, risk assessments, and gap analysis. For developed programs we provide clinical trial and support through a network of medical teaching institutions and hospitals.