Saturday, September 04, 2010
 
Clinical Project Management
Clinical Site Monitoring
Data Management
Medical Monitoring
Medical Writing
Quality Assurance / Auditing
Site Selection / Patient Recruitment
Biostatistics
IT Consultancy
Training
Support for Late-Phase Studies
SOP Development

Training Courses

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ClinArt International cooperates with The Association of Clinical Research Professionals (www.ACRPnet.org) to bring well known Industry speakers to deliver training sessions in the region.  All our courses are allocated Continuous Medical Points by Harvard Medical School Dubai Centre.
 
  Some of our courses are as below:
   
 
  Course Title Duration  
  Fundamentals of Clinical Research 1 to 2 days  
  Intermediate CRA Training 2 days  
  Intermediate CRC Training 2 days  
  GCP 1 to 2 days  
  Project Management 2 days  
  Project Management for Clinical Research Coordinators 2 days  
  Certification Exam Review for CRA, CRC, and CPI 1 day  
  Certification Exam Review for CRAs 2.5 hrs  
  Ethics 1/2 to 1 day  
  Development of Investigational Products 1 day  
  The European Clinical Trials Regulations 1/2 day  
  Ethics and Management for Independent Ethics Committees 1/2 to 2 days  
  Ensuring Successful Trials 1 day  
  Electronic Data Capture 1/2 to 1 day  
  Compliance and Inspections 1/2 to 2 days  
  Fraud & Misconduct 1/2 day  
  FDA & the Clinical Investigator 1 day  
  Enhancing Patient Participation In Clinical Trials 1 day  
  Business Development:  Budgeting and Contract Management 2 days  
  Successful Strategies for Medical Device Clinical Trials 1 day  
  SOPs for Investigator Sites 1 day  
  Informed consent 1/2 day  
  Patient recruitment 1/2 day  
  A day in the life of a study coordinator 2 hrs  
  The UK Healthcare Marketplace 1 to 4 days  
  Data Management 1 to 2 days  
  Performing Paediatric Trials 1 day  

 

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