Clinical Study Designs

Clinical study design is the formulation of trials and experiments, as well as observational studies in medical, clinical and other types of research involving human beings. Clinical trials are typically conducted in four phases, each phase is considered as separate trial and, after completion of a phase, investigators are required to submit their data for approval from the FDA before continuing to the next phase. Types of study designs are Meta-Analysis, Systematic Review, Randomized Controlled Trial, Cohort Study, Comparative Study, Case-control Study, Cross-sectional study, Case Reports and Series, Animal Research Studies, Test-tube Lab Research

  • Design and end points of clinical trials
  • Trial design: formulation development, manufacturing and analytical testing
  • Observational study designs
  • Experimental Study designs
  • Randomized Clinical Trials
  • Adaptive Clinical Trials
  • Patient consideration and patient oriented trial designs
  • Trial and protocol designs that reflects patient considerations
  • Randomized placebo- controlled trials
  • Maximizing Trial Success Through Patient–Oriented Study Designs

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May 08-10, 2017

10th Asia-Pacific Pharma Congress

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16th Annual Medicinal & Pharmaceutical Sciences Congress

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9th Annual Congress on Drug Design & Drug Formulation

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A B2B Networking & Global Knowledge Exchange Forum

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