Overview of Clinical Trials

COURSE DETAILS

5 May 2014, Singapore 9.00am - 5.00pm (Reg. from 8.30am)
Singapore

Normal Course Fee: $979
Early Bird Special: $929 (Before 4 April 2014)
Group (>3): $899

 

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THE PROGRAM

This interactive one day workshop will cover a complete overview of the clinical trial process. Gain a clear understanding of the different phases of clinical research and how does clinical research fit into how a drug is developed internationally. Gain an understanding on the roles and responsibilities of key members of a Trial. This course also provides a step by step guide to how clinical trials are set up and run globally, including meeting the Clinical Trial Directives and the new GCP Directives, special considerations for running international clinical trials, data management in trials and regulatory controls.

 

COURSE OBJECTIVE

  • Understand how does clinical research fit into how a drug is developed internationally
  • Gain a clear picture of the different phases of clinical research
  • Understand the terminology and the key tools of clinical research
  • Understand the roles and responsibilities of the key people involved in clinical trial
  • Gain knowledge on how clinical trials are set up and run globally
  • Know what is required for clinical trials to meet the Clinical Trials Directives and the New GCP directives
  • Understand how data from Clinical Trials is managed
  • Learn about regulatory control of international clinical trials
  • Gain insight into the special considerations for running clinical trials internationally

 

WHO SHOULD JOIN

  • Professionals that wish to have an complete overview of the clinical trials
  • Anyone with little or no Knowledge about clinical research

 

Distinguished Trainers

Dr Lisa H Butler
D.Phi (PhD), BSc (Hons), FICR, CSci

Dr Butler has over 17 years of experience in the clinical research industry.  She has extensive expertise in the fields of Project Management, Ethics and Regulatory Submissions (UK and Republic of Ireland). Dr Butler obtained her PhD in Clinical Medicine from Oxford University in 1997. Dr Butler has extensive experience in monitoring and clinical project management having worked with multi-national companies like Novartis, Bio Products Laboratory, Covance, amongst many others.  She is an experienced trainer having responsible for the training for new and site staffs on areas of ICH GCP, Monitoring Skills and therapeutic areas. Read More