Program strategies and efficiencies Archives - Page 2 of 3 - Pharmetheus

Overview of Authorized Drug Products for Subcutaneous Administration: Pharmaceutical, Therapeutic, and Physicochemical Properties

Applications of Clinically Relevant Dissolution Testing: Workshop Summary Report

Dissolution and Translational Modeling Strategies Toward Establishing an In Vitro-In Vivo Link-a Workshop Summary Report

Assessment of Expected Drug Exposure Relative Maximum Safety Limits in Early Phase Studies

A Regulatory View on Dose Finding Studies and on the Value of Dose-Exposure-Response Analysis

Open Innovation: Towards Sharing of Data, Models and Workflows

Reproducible Reporting

Population PKPD Analysis of CD4 and ACR Response after SC Administration of Tregalizumab to Patients with Rheumatoid Arthritis

Application of a Multi-Criteria Decision Analysis Model in the Dose Selection of Combination Therapy for Overactive Bladder

Modelling and Simulation of Neurological Endpoints (Modified Rankin Scale [mRS] and National Institute of Health Stroke Scale [NIHSS]) to Aid Clinical Trial Design in Intracerebral Hemorrhage (ICH)

Characterizing Variability in Warfarin Dose Requirements in Children Using Modelling and Simulation

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