Our GOOD CLINICAL PRACTICE (GCP) Course 2009 is now open for registration. The purpose of the GCP course is to provide training and understanding for personnel involved in the design, conduct, documentation, and reporting of clinical trials. As clinical trials involve human subjects, much attention is drawn on the ethical issues surrounding trials from the society like the health authorities, the general public, and the media. The GCP course will address and outline how the rights, safety, and well being of trial subjects can be protected. So do hurry and register with us!!!! Come join us at SGH Postgraduate Medical Institute (PGMI), Block 6, level 1, lecture rooms 3 & 4 on 15/01/2009 & 16/01/2009 (Thursday & Friday). Program Day 1 Day 2 Drug Development Process Clinical Trial Safety (Adverse Events and Serious Adverse Events) Clinical Trial Process and Practice Investigational Product Management Regulatory Requirements of Clinical Trials Case Study / Quiz Ethics Committees in Singapore Responsibilities of the Sponsor Clinical Trial Agreement and Budget Management Monitoring and Data Management Organizing and Maintaining the Investigator’s File Quality Assurance and Audits Investigator’s Responsibilities Fraud and Misconduct in Clinical Trial Informed Consent Documents and Process Case Study / Quiz As this course is on a first-come first-served basis with limited seats, we strongly encourage participants to register with us early. Certificate of Participation will be given out to all who attend the course on both days. The course fee is $80. Applications for CME, CNE & CPE Points have been submitted and subjected to approval. Lunch and tea breaks will be provided on both days. To register, kindly fill up the registration form. Deadline for the registration will be on 19 Dec 2008 (Friday). Feel free to email to research.secretariat@sgh.com.sg if you have any enquiries pertaining to the workshop. Workshop organised by: Division of Research and Clinical Trials Resource Centre, Singapore General Hospital