The next generation of technology for clinical trials

Clintara provides rater training and certification for clinical trials, site independent assessment programs to assure in-study data quality and consistency, and consulting services for the pharmaceutical and clinical research industries.

Our Solutions

Rater Training and Certification
Subjective endpoints are the hallmark of CNS trials, and the instruments...[Read More...]

Ratings Diligence
Over and above a strong foundation of rater training and certification, CNS trial success is contingent...[Read More...]

Clinical Study Consulting
With only one in five new drugs making it from phase I to market...[Read More...]

Research/Publications

Validation of a Global Assessment Measure for Fatigue

Validation of a Global Assessment Measure for Fatigue Steven D. Targum, Howard Hassman, Maria … [Read More...]

The rationale for site-independent review

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Targeted scoring criteria reduce variance in global impressions

This study examined the confounding effect of treatment emergent physical or psychic symptoms on … [Read More...]

Redefining Affective Disorders: Relevance for Drug Development

The evaluation of new drug entities with specific modes of action may be hampered by rigid … [Read More...]

Clinical Study Design and Consulting Services

Led by Steven D. Targum MD, our scientific services group assists sponsors with protocol development, rating scale development, and other specialized scientific consulting services.

Clintara has collaborated on the development of two instruments being used on several studies, the CGI for Fatigue, and the Clinical Validation Inventory for Study Admission (C-VISA©)...[Read More...]

C-VISA is copyright Clintara, LLC.

“Dual” Scoring Clinical Ratings

The Clintara strategy asserts that site-independent clinical data review for diagnostic verification, subject validation, and symptom severity confirmation can enhance the subject selection process and optimize clinical trial outcomes.

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