Ch-3 Bioavailability of Drugs and Bioequivalence-18th Batch
Clinical trials
Writing a Study Protocol for Therapeutic Recreation Studies in Canada
Animal models for screening of antiepileptic drugs &
Bioavailability o Fdisperse Dosage Form
Quality by Design for Topical Dosage Forms Robert Lionberger Office of Generic Drugs.
1 Issues in Selection of Deltas in Non-Inferiority Trials : Acute Bacterial Meningitis and Hospital- Acquired Pneumonia John H. Powers, M.D. Medical Officer.
Design and Statistical Analysis of Thorough QT (TQT) Studies Yi Tsong, Ph.D., CDER/FDA Co-author – Joanne Zhang, Ph.D., CDER/FDA The opinions presented.
Current Regulatory Challenges in conduct of Clinical Trials –India Prabhat Kumar November 2014.
Analysis of Clinical Trials in Children Registered in the Clinical Trials Registry of India S. Manikandan*, M. Jayanthi*, B. Gitanjali** and G. Sivagnanam*
Neuro Block 4 Questions
Analysis of Clinical Trials in Children Registered in the Clinical Trials Registry of India