Clinical development

• Medical Communications 2012
  Emne: Clinical development, Medical writing, Communication skills, Patient information
  Udbyder: DIA
  Sted: Orlando, FL, USA
  Dato: 5-7 March 2012
  
• Non-clinical Safety and Toxicology
  Emne: Clinical development, Clinical research, Product development, Clinical trials, Bio markers, Lab data, Project management, Safety, Product development, Clinical pharmacology, Drug discovery
  Udbyder: KU, FARMA
  Sted: Copenhagen, Denmark
  Dato: 7-11 May 2012
  
• Scientific Writing – a framework for writing a scientific paper
  Emne: Clinical development, Medical writing, Communication skills, Expert reports, Scientific documents
  Udbyder: KU, FARMA
  Sted: Copenhagen, Denmark
  Dato: 15 May 2012
  
• Clinical Evaluation of Drug Products
  Emne: Clinical development, Medical writing, Protocols, Clinical trials, Learning, General conditions, Clinical research, QA
  Udbyder: KU, FARMA
  Sted: Copenhagen, Denmark
  Dato: 21-25 May 2012
  
• 6th Annual Clinical Forum
  Emne: Clinical development, Clinical research, Clinical trials, Regulation, Clinical trials, General conditions
  Udbyder: DIA
  Sted: The Hague, The Netherlands
  Dato: 8-10 October 2012
  
• DIA Practical GCP Compliance Auditing of Trials and Systems Training Course
  Emne: Clinical development, Clinical trials, Monitoring / audit, GCP, Inspection
  Udbyder: DIA
  Sted: London, England
  Dato: 17-19 October 2012
  

Courses from other providers

• ARCHIVED WEBINAR: Evaluating IRBs: Finding an IRB that is Compliant, Provides High Quality and Customer Service
  Emne: Clinical development, Clinical trials, IRB
  Udbyder: DIA
  Sted: Internet
  Dato: Available April 14, 2011 through April 13, 2012
  
• MEDDEV training ISO 14155 for Clinical Research Associates
  Emne: Clinical development, Clinical trials, Regulatory affairs, Regulation, CRA, Positions - in detail, CRA
  Udbyder: ECCRT
  Sted: Brussels, Belgium
  Dato: 1) 26 January 2) 11 June 3) 6 October 4) 2 November 2012
  
• How to be an Effective CTA
  Emne: Clinical development, Positions - in detail, CTA
  Udbyder: ROSTRUM
  Sted: London, England
  Dato: 1) 6 February 2) 10 September 2012
  
• Monitoring Clinical Drug Studies: Beginner
  Emne: Clinical development, Clinical trials, Monitoring / audit
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 20-22 February 2012
  
• Preparation, Packaging and Labeling of Clinical Trial Materials
  Emne: Clinical development, Trial support, Distribution, Labelling / packaging
  Udbyder: CfPA
  Sted: Amsterdam, The Netherlands
  Dato: 20-21 February 2012
  
• Monitoring Safety in Clinical Trials and Drug Development
  Emne: Clinical development, Clinical trials, Safety, Monitoring / audit
  Udbyder: DSRU
  Sted: London, England
  Dato: 22-23 February 2012
  
• Good Clinical Practice Auditing - Principles and Practice
  Emne: Clinical development, Clinical trials, Monitoring / audit
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 28-29 February 2012
  
• Optimising Paediatric Drug Design & Development
  Emne: Clinical development, Product development, Drug discovery, Clinical research, Clinical research, Product development, Clinical trials, Children
  Udbyder: Marcus Evans
  Sted: Amsterdam, The Netherlands
  Dato: 29 February - 2 March 2012
  
• Good Clinical Practice for the Laboratory Scientist
  Emne: Clinical development, Clinical trials, GCP
  Udbyder: Barnett International
  Sted: San Diego, CA, USA
  Dato: 1 March 2012
  
• Developing Clinical Study Budgets
  Emne: Clinical development, Clinical trials, Economy / contracts, Clinical research, Economy
  Udbyder: Barnett International
  Sted: San Diego, CA, USA
  Dato: 1 March 2012
  
• Source Documentation
  Emne: Clinical development, Clinical research, Clinical trials
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 9 March 2012
  
• Study Site Start-Up
  Emne: Clinical development, Clinical trials, Investigational site, Project management
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 9 March 2012
  
• The CRA Manager
  Emne: Clinical development, Positions - in detail, CRA manager, Clinical research, CRA, Clinical trials, CRA
  Udbyder: Barnett International
  Sted: San Fransisco, CA, USA
  Dato: 15-16 March 2012
  
• MEDDEV training ISO 14155 for Investigators
  Emne: Clinical development, Clinical trials, EU regulation, Regulation, General conditions
  Udbyder: ECCRT
  Sted: Brussels; Belgium
  Dato: 1) 19 March 2) 3 November 2012
  
• Oncology Clinical Trials
  Emne: Clinical development, Clinical trials, Cancer
  Udbyder: ROSTRUM
  Sted: London, England
  Dato: 1) 21 March 2) 24 September 2012
  
• Medical Terminology for Clinical Research Professionals
  Emne: Clinical development, Medical writing, Scientific documents, Clinical research, QA
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 10-11 April 2012
  
• Report Writing for CRAs
  Emne: Clinical development, Medical writing, Communication skills, Expert reports, Trials reports, Site visit reports, Positions - in detail, CRA
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 13 April 2012
  
• Statistical Concepts for Non-Statisticians
  Emne: Clinical development, Statistics, Clinical trials, Introduction, Trial design
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 16-17 April 2012
  
• Comprehensive CRC Training
  Emne: Clinical development, Positions - in detail, CRC
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 26-27 April 2012
  
• Planning and Conducting Global Clinical Trials
  Emne: Clinical development, Clinical trials, Administration, Study coordinator, Trial subjects, Multicenter, Developing countries, Project management, General conditions
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 26-27 April 2012
  
• Conducting Clinical Trials Under ICH GCP
  Emne: Clinical development, Clinical research, GCP, Clinical trials, ICH
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 3-4 May 2012
  
• Global GCP Monitoring
  Emne: Clinical development, Clinical trials, Monitoring / audit, Clinical research, GCP
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 3-4 May 2012
  
• Patient Registry Programs
  Emne: Clinical development, Clinical research, Patient registry
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 3-4 May 2012
  
• The Highly Effective CRA
  Emne: Clinical development, Clinical research, CRA, Clinical trials, CRA, Positions - in detail, CRA manager, CRA
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 8-9 May 2012
  
• Clinical Trials for Pharmaceuticals: Design and Development
  Emne: Clinical development, Clinical trials, Trial design, General conditions, Clinical research, Clinical trials, Product development, Product development, Clinical trials
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 9-10 May 2012
  
• Mastering Cost Management for Global Clinical Trials
  Emne: Clinical development, Clinical trials, Economy / contracts, Management
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 9-10 May 2012
  
• Advanced GCP
  Emne: Clinical development, Clinical research, GCP
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 4-5 June 2012
  
• Clinical Project Management: Intermediate
  Emne: Clinical development, Clinical research, Project management, Clinical trials, Project management
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 4-5 June 2012
  
• Data Management in the Electronic Data Capture Arena
  Emne: Clinical development, Data management, QA, Regulation, Computer systems, Positions - in detail, Clinical data manager
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 5-6 June 2012
  
• Introduction to Clinical Data Management
  Emne: Clinical development, Data management, Regulation, Computer systems, QA, Introduction, Clinical trials, QA, Clinical research, QA
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 14-15 June 2012
  
• CRA & CRC Beginner
  Emne: Clinical development, Clinical research, CRA, Positions - in detail, CRC
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 18-20 June 2012
  
• Query Creation
  Emne: Clinical development, Data management, Introduction, Regulation, Medical writing, Protocols
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 20 June 2012
  
• European GMPs and the Role of the QP
  Emne: Clinical development, Positions - in detail, QP
  Udbyder: ECA
  Sted: Bethesda, MD, USA
  Dato: 27-28 June 2012
  
• Root Cause Analysis & Corrective and Preventive Action in Site Management
  Emne: Clinical development, Clinical trials, CRO, Investigational site, IRB
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 28-29 June 2012
  
• Coordinator Intermediate Level
  Emne: Clinical development, Clinical trials, Protocols, Economy / contracts, Project management, Study coordinator, SOP, Sponsor, International regulation, ICH, GCP, Lab data, Learning, Monitoring / audit
  Udbyder: Aureus Research Consultants
  Sted: A) To be announced B) Internet/CD-ROM
  Dato: A: Classes) To be announced B) Internet/CD-ROM: Multiple dates
  
• FDA Inspections: What You Can Expect in an Audit (Online Course)
  Emne: Clinical development, Clinical trials, International regulation, Monitoring / audit, Study coordinator, Inspection, Regulatory affairs, Clinical trials, International regulation
  Udbyder: Aureus Research Consultants
  Sted: Internet
  Dato: Multiple dates
  
• Coordinator Entry Level
  Emne: Clinical development, Positions - in detail, CRC
  Udbyder: Aureus Research Consultants
  Sted: Internet
  Dato: Multiple dates
  
• Biostatistics
  Emne: Clinical development, Statistics, Trial design, Evaluation
  Udbyder: Boston University
  Sted: Internet
  Dato: Ongoing
  
• Design and Conduct of Clinical Trials
  Emne: Clinical development, Clinical trials, General conditions
  Udbyder: Boston University
  Sted: Internet
  Dato: Ongoing
  
• Good Clinical Practices for Clinical Research (GMS CI 660 OL)
  Emne: Clinical development, Clinical trials, General conditions, GCP, Regulation
  Udbyder: Boston University
  Sted: Internettet
  Dato: Ongoing
  
• How to Conduct Clinical Trails
  Emne: Clinical development, Clinical trials, General conditions
  Udbyder: CRTO
  Sted: Internet
  Dato: Multible dates
  
• Monitoring Clinical Studies
  Emne: Clinical development, Clinical trials, Monitoring / audit
  Udbyder: CRTO
  Sted: Internet
  Dato: Multible dates
  
• Statistics for non-statisticians
  Emne: Clinical development, Statistics, Introduction, Specialised analysis
  Udbyder: CRTO
  Sted: Internet
  Dato: Ongoing
  
• Database Management
  Emne: Clinical development, Data management, Introduction
  Udbyder: DIA
  Sted: Internet
  Dato: Ongoing
  
• Informed Consent
  Emne: Clinical development, Clinical trials, HIPAA, Trial subjects, Recruitment
  Udbyder: DIA
  Sted: Internet
  Dato: Ongoing
  
• Medical Writing
  Emne: Clinical development, Medical writing, Communication skills
  Udbyder: DIA
  Sted: Internet
  Dato:
  
• Complying with the HIPAA Privacy Rule in Research
  Emne: Clinical development, Clinical trials, HIPAA
  Udbyder: Medical Research Management
  Sted: Internet
  Dato: Ongoing
  
• Applied Good Clinical Practices
  Emne: Clinical development, Clinical trials, GCP, QA
  Udbyder: PERI
  Sted: Online
  Dato: Ongoing
  
• Clinical Monitoring and Site Management
  Emne: Clinical development, Clinical trials, Monitoring / audit, International regulation, GCP, ICH
  Udbyder: PERI
  Sted: Internet
  Dato: Ongoing
  
• Fundamentals of Site Management and Clinical Monitoring
  Emne: Clinical development, Clinical trials, Monitoring / audit, GCP, Management
  Udbyder: PERI
  Sted: Internet
  Dato: Ongoing
  
• Good Clinical Practices for the Clinical Research Team
  Emne: Clinical development, Clinical trials, General conditions, GCP, Regulation
  Udbyder: PERI
  Sted: Internet
  Dato: Ongoing
  
• Pharmacology Online: The Fundamental Principles
  Emne: Clinical development, Clinical research, Medicine
  Udbyder: PERI
  Sted: Internet
  Dato: Ongoing
  
• Statistical Concepts Used in Clinical Trials
  Emne: Clinical development, Statistics, Trial design, Evaluation
  Udbyder: PERI
  Sted: Internet
  Dato: Ongoing
  
• Good Clinical Practices (GCPs)
  Emne: Clinical development, Clinical trials, GCP
  Udbyder: RAPS
  Sted: Internet
  Dato: Ongoing
  
• Biostatistics with special emphasis on clinical trials
  Emne: Clinical development, Statistics, Clinical trials
  Udbyder: Uppsala Universitet
  Sted: Internet
  Dato: 2 weeks, any time during semester
  
• Methodology in clinical trials
  Emne: Clinical development, Clinical trials, General conditions, Children, CRO, Multicenter, Monitoring / audit, Phase I, Phase III, Phase IV, Phase II, Trial design, GCP, Inspection, QA, Recruitment, SOP, Study reports
  Udbyder: Uppsala Universitet
  Sted: Internet
  Dato: 2 weeks, any time during the semester
  
• Clinical trial monitoring: Site evaluation and set-up
  Emne: Clinical development, Clinical trials, CRA, Investigational site, QA, General conditions, Regulation, ICH, GCP, Inspection, Monitoring / audit
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• Clinical trial monitoring: Study monitoring, documentation and closure
  Emne: Clinical development, Clinical trials, CRA, Monitoring / audit, QA, ICH, GCP, Inspection, Investigational site, General conditions, Project management
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• How to Obtain Approval to Conduct Clinical Trials in the EU
  Emne: Clinical development, Clinical trials, Ethics, Regulation
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• Introduction to Clinical Trial Preparation and Design
  Emne: Clinical development, Clinical trials, General conditions
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• Introduction to Clinical Trials and Drug Development
  Emne: Clinical development, Clinical trials, General conditions, Ethics, Regulation, Product development, Clinical trials
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• Introduction to Clinical Trials in India
  Emne: Clinical development, Clinical trials, Developing countries
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• Introduction to ICH Good Clinical Practice (ICH-GCP)
  Emne: Clinical development, Clinical trials, GCP, General conditions
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing
  
• Pharmacokinetics and Pharmacodynamics in Drug Registration
  Emne: Clinical development, PK/PD, PK, PD, Clinical pharmacy, PK / PD, PK, PD, Regulatory affairs, Regulatory affairs, Clinical documentation
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing