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	Title	Author(s)	Issue Date
	Study Site Standard Operating Procedure SOP: S1 - Site description Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study site standard operating procedures	Thorburn, J Tam, SYM Yan, YSM Karlberg, JPE Other(s):University of Hong Kong. Faculty of Medicine. Clinical Trial Centre.	2000
	Study Site Standard Operating Procedure SOP: QA2 - Study-specific inspection Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA4 - Human research protection program Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA5 - Fraud and misconduct Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA6 - Confidentiality agreement, obligations and practices Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA7 - Participant’s complains Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA8 - Emergency resuscitation - Cardiac arrest Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA9 - Trial registry Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA10 - Conflict of interest resolution Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA11 - Feasibility study Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: QA12 - Dissemination of study results Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: P13 - Regulatory authority applications and documents Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Study Site Standard Operating Procedure SOP: P14 - Vulnerable subjects Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2010
	Clinical Trial Protocol Development - Essential Elements Highlight Proceeding/Conference:HA Training Symposium on Clinical Research Compliance: Clinical Research Planning	Tam, SYM	2015
	Quality Control for Sponsored and Investigator-initiated Clinical Studies Proceeding/Conference:HA Training Symposium on Clinical Research Compliance: Clinical Research Planning	Tam, SYM	2015
	Efficient and Effective Ethics Committee Application for Clinical Trials Proceeding/Conference:Meeting of the Drug Information Association, DIA 2000	Tam, SYM Thorburn, J Karlberg, JPE	2000
	Study Site Standard Operating Procedure SOP: P3 review of protocol amendments Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, S	2009
	Preparing and Updating Study Site Standard Operating Procedures Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2009
	Study Site Standard Operating Procedure SOP: P4 Review of Investigator’s Brochure Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2009
	Study Site Standard Operating Procedures Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2009
	Study Site Standard Operating Procedure SOP: P2 Review Of Protocol Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2009
	Study Site Standard Operating Procedure SOP: P1 Pre-Study Visit Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2009
	Study Site Standard Operating Procedure SOP: P5 Review of Case Report Form (CRF) Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2009
	Study Site Standard Operating Procedure SOP: T4 Investigational Products Accounting, Dispensing and Administration Journal:Clinical Trial Magnifier	Karlberg, JPE Tam, SYM	2010