Clinical Trials and Drug Risk Assessment

Master

Online

£ 785 VAT inc.

Description

  • Type

    Master

  • Methodology

    Online

  • Duration

    3 Weeks

  • Online campus

    Yes

  • Delivery of study materials

    Yes

  • Support service

    Yes

  • Virtual classes

    Yes

A clinical trial is an exceedingly important instrument in the assessment of treatment efficacy. With regard to clinical trials, the emphasis will be on methodological principles and on the clinical practice of therapeutic experiments. This online medical course addresses the principles of studying the effects of drug treatments on the risks of unintended effects. The accent is on proper formulation of the research problem with a view to clinical and regulatory relevance of the study results, and on requirements for validity in non-experimental research.

About this course

The course program provides a thorough medical education into the field of clinical trials, covering the principles of therapeutic research design, including design of study, design of data collection, design of data analysis, including some modelling techniques in the analysis to clinical trials, and the interpretation of its results. The program also touches on the principles of drug risk assessment in the context of therapeutic research.

Questions & Answers

Add your question

Our advisors and other users will be able to reply to you

Who would you like to address this question to?

Fill in your details to get a reply

We will only publish your name and question

Reviews

Subjects

  • Risk Assessment
  • Risk
  • Design
  • IT risk
  • Randomized
  • Controlled
  • Data analysis
  • Principles
  • Assessment

Course programme

By the end of the course, you should be able to:
  • Explain the basic design principles of a randomized controlled trial
  • Describe specialized design options for a randomized controlled trial
  • Apply the basic principles of data analysis of a randomized controlled trial
  • Describe the principles of advanced data analysis of a randomized controlled trial
  • Explain the principles of drug risk assessment and how to evaluate potential side effects of medication
  • State common practical issues in the conduct of a randomized controlled trial and suitable solutions
  • Design a valid randomized controlled trial for any intervention
  • Interpret scientific papers on randomized controlled trials

Clinical Trials and Drug Risk Assessment

£ 785 VAT inc.