Training Courses Conducted

Training Courses conducted by Debbie Jordan

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NAME: Debbie Jordan          
POSITION: Medical Writer and Clinical Research Consultant

Date

Training course

Client

Content
2010 Writing the Clinical Study Report PharmaSchool 2-day training course
2010 The CTD Clinical Summary EMWA A review of the guidelines for the CTD Clinical Summary
2010 Writing the Clinical Study Report Rostrum 1-day training course
2009 The CTD Clinical Overview EMWA A review of the guidelines for the CTD Clinical Overview
2008 Improving your medical writing skills Rostrum 1-day training course
2008 Time Management EMWA Three-hour session on time management techniques
2008 The CTD Clinical Summary (two courses) EMWA A review of the guidelines for the CTD Clinical Summary
2006 Scientific Writing Skills EMEA Two 1-day training courses on scientific writing
2006 Introduction to medical writing (two courses) Rostrum All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
2006 SOP training Millennium Training given on general company SOPs and Clinical Operations procedures. 
2006 Time Management EMWA Three-hour session on time management techniques
2006 The CTD Clinical Overview EMWA A review of the guidelines for the CTD Clinical Overview
2006 CSRs and the ICH E3 guidelines TOPRA Course as part of the TOPRA professional training programme (for Regulatory Affairs personnel)
2005 EU Directive Millennium Training given EU Directive 2005/28/EC
2005 Time Management EMWA Three-hour session on time management techniques
2005 The CTD Clinical Overview EMWA A review of the guidelines for the CTD Clinical Overview
2005 GCP training Millennium Training given on ICH GCP and the EU Clinical Trials Directive.  Course given twice in 2005.
2005 SOP training Millennium Training given on general company SOPs and Clinical Operations procedures.  Course given twice in 2005.
2005 Effective medical writing
(two courses)		 Rostrum All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
2004 GCP training Millennium Training given on ICH GCP and the EU Clinical Trials Directive 2001/20/EC.  Course given 3 times in 2004.
2004 SOP training Millennium Training given on general company SOPs and Clinical Operations procedures.  Course given 3 times in 2004.
2004 Effective medical writing Fujisawa All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
2004 Effective medical writing
(two courses)		 Rostrum All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
2003 CSRs and the ICH E3 guidelines BIRA Course as part of the BIRA professional training programme
2002 Medical Writing Workshop Aventis Pasteur CSRs and the ICH E3 guidelines
2002 GCP ClinTrials Research Introductory training for new staff
2002 Effective medical writing ClinTrials Research All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
2002 Introduction to the Pharmaceutical Industry ClinTrials Research Introductory training for new staff
2001 Effective medical writing PRA All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
2001 Introduction to the Pharmaceutical Industry PRA Introductory training for new staff
2000 Effective medical writing Rostrum All aspects of medical writing, including protocols, CSRs, manuscripts and the related guidelines
1999-2000 First steps for the new monitor Covance Introductory training for new CRAs
1999-2000 Clinical Jargon Covance Basic introduction to clinical research
1996-1999 Medical Writing and Clinical Research ClinTrials Research Ongoing training programme for all medical writing staff on various aspects of medical writing, clinical research, time management etc.
1994-1995 Total Quality Management Cyanamid All aspects of TQM to all staff