Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the human subjects of research; providing regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects

'advic':35 'clinic':5,48,63 'complianc':28,58 'concern':36 'consult':29 'develop':40 'dilig':38 'due':37 'ensur':18 'field':46 'human':8,22,51,66 'independ':2,60 'inform':16,54 'involv':7,50,65 'name':10 'natur':33 'polici':43 'protect':19 'protocol':13 'provid':1,26,53 'regulatori':27,42,57 'relat':15,55 'research':12,25 'review':3,11,61 'servic':30 'strateg':39 'subject':9,23,52,67 'trial':6,49,64

Non-downloadable software for use by clinical researchers, research sponsors and clinical research organizations for use in automating the submission, review and approval process of human subject clinical research projects

'approv':24 'autom':19 'clinic':8,13,29 'download':3 'human':27 'non':2 'non-download':1 'organ':15 'process':25 'project':31 'research':9,10,14,30 'review':22 'softwar':4 'sponsor':11 'subject':28 'submiss':21 'use':6,17

W WCG IRB

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