| Clinical Trial Training Courses and Conferences |
|
start
date |
sponsor |
clinical trial
training courses and conferences |
location |
Thursday, December 1, 2011 |
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Ensure the Safety of Clinical Trials: The Roles of Data Safety Monitoring Boards (DSMB) and Institutional Review Boards (IRB) - Webinar By GlobalCompliancePanel
Sponsor: | DE, United States |
3/9/2010 |
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Electronic Data Capture (EDC) and Electronic Health Record (EHR) in Clinical Trials: Collecting and Leveraging Data to Optimize Clinical Trials
Sponsor: | California, United State Of America |
3/30/2010 |
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The Importance of ICH Guidelines and its Role in Achieving Good Clinical Practice
Sponsor: | California, United State Of America |
3/3/2010 |
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Decoding CLIA (Clinical Laboratory Improvement Amendments) Regulations: Calibration, Calibration Verification and Method Validation
Sponsor: | California, United State Of America |
3/24/2010 |
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How to Create and Understand A Statistical Analysis Plan for A Clinical Study
Sponsor: | California, United State Of America |
3/17/2010 |
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Evaluating Clinical Sites: going beyond regulatory requirements to ensure success
Sponsor: | California, United State Of America |
3/10/2010 |
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Mastering the Art of Clinical Monitoring with Enhanced Techniques - Getting Beyond the Basics
Sponsor: | California, United State Of America |
12/14/2010 |
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How to Set up Data Monitoring Committees (DMCs / DSMBs) and what is effect on the Drug Development Process - Clinical Webinar By ComplianceOnline
Sponsor: | CA, USA |
12/13/2007 |
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Clinical and Laboratory Genomic and Genetic Standards
Sponsor: DIA Drug Information Association | MD, USA |
12/10/2010 |
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CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment - Laboratory Webinar By ComplianceOnline
Sponsor: | CA, USA |
12/10/2010 |
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How to investigate environmental monitoring excursion limits - Clinical Webinar By ComplianceOnline
Sponsor: | CA, USA |
12/10/2007 |
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Laboratory Analysis in Clinical Trials
Sponsor: CFPA The Center for Professional Advancement | , The Netherlands |
12/10/2007 |
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Good Clinical Practices
Sponsor: The Center for Professional Innovation & Education | PA, USA |
12/05/2007 |
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Pharmacokinetics and Pharmacodynamics: Principles and Applications in Pre-Clinical Drug Development
Sponsor: American Chemical Society | CA, USA |
12/05/2006 |
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The Quest to Enable the Electronic Clinical Trial: Finding Clarity in a Confusing World
Sponsor: Drug Information Association (DIA) | MD, USA |
12/04/2006 |
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Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Information Association (DIA) | AZ, USA |
12/04/2006 |
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Identifying and Validating Metabolic Markers for Drug Development and Clinical Studies
Sponsor: Cambridge Healthtech Institute | FL, USA |
12/03/2010 |
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Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Clinical Webinar By ComplianceOnline
Sponsor: | CA, USA |
12/02/2009 |
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The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation and Education | CA, USA |
11/30/2010 |
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Ethics, Standards and Identifying Risks in Clinical Research - Clinical Webinar By ComplianceOnline
Sponsor: | CA, USA |
11/30/2009 |
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Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation and Education | CA, USA |
11/27/2007 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | PA, USA |
11/27/2006 |
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Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: The Center for Professional Advancement (CfPA) | amsterdam, the netherlands |
11/27/2006 |
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Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: The Center for Professional Advancement (CfPA) | amsterdam, the netherlands |
11/27/2006 |
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Pharmacovigilance Training: Clinical Trials and Marketed Products
Sponsor: Drug Information Association (DIA) | , France |
11/21/2007 |
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Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: CFPA The Center for Professional Advancement | , The Netherlands |
11/18/2007 |
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DIA, ICRI, AND BCI 2nd Annual Conference on DRUG DISCOVERY AND CLINICAL DEVELOPMENT IN INDIA Scientific Platform for global Regulatory Landscape through Biologics and Medical Devices
Sponsor: DIA Drug Information Association | , India |
11/16/2009 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation and Education | PA, USA |
11/15/2011 |
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Biomarker Application for Improved Clinical Trial Outcomes
Sponsor: | MA, USA |
11/13/2007 |
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Winning Strategies for Achieving a Quality EDC Clinical Trial Process - Sponsor/CRO, Investigator, IRB Approver and IT/IS
Sponsor: DIA Drug Information Association | FL, USA |
11/13/2007 |
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Clinical Trial Disclosure learning the landscape and reading the roadmap
Sponsor: DIA Drug Information Association | FL, USA |
11/12/2007 |
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Regulatory Affairs in Medical Device Clinical Trials
Sponsor: Q1 Productions.com | Az, USA |
11/12/07 |
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Good Laboratory Practices for Pre-Clinical Testing, Compliance, QA & Audit
Sponsor: The Center for Professional Innovation & Education | PA, USA |
11/07/2006 |
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Beyond 2006 - Software and Services Trends for eClinical Trials
Sponsor: Drug Information Association (DIA) | PA, USA |
11/05/2007 |
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Early Stage Clinical Development
Sponsor: CFPA The Center for Professional Advancement | , The Netherlands |
11/05/2007 |
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Clinical Statistics for NonStatisticians
Sponsor: DIA Drug Information Association | , Ireland |
11/05/2006 |
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The Changing World of Clinical Trials - European Clinical Research Conference, European eClinical Conference, 16th Annual European CDM Conference
Sponsor: Drug Information Association (DIA) | , Switzerland |
11/05/2006 |
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DIA Multi-Track Conference on CDM, eClinical & Clinical Research
Sponsor: Drug Information Association (DIA) | Basel, Switzerland |
11/02/2009 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation and Education | PA, USA |
11/01/2007 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | PA, USA |
11/01/2006 |
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Innovation and Reform in Clinical Trials
Sponsor: Cambridge Health Institute | Ontario, Canada |
10/30/2006 |
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Development of a Clinical Study Report
Sponsor: Drug Information Association (DIA) | PA, USA |
10/29/2009 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation and Education | PA, USA |
10/29/2007 |
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Outsourcing Preclinical Toxicology Studies
Sponsor: The Center for Professional Innovation & Education | PA, USA |
10/26/2010 |
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6th Annual Future of Clinical Trials
Sponsor: | Vienna, |
10/24/2006 |
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Preclinical Disease Model
Sponsor: Cambridge Health Institute | MA, USA |
10/23/2006 |
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Advanced Clinical Statistics for Nonstatisticians
Sponsor: Drug Information Association (DIA) | PA, USA |
10/22/2009 |
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Understanding Regulatory & Clinical Information Systems During Product Development
Sponsor: The Center for Professional Innovation and Education | PA, USA |
10/20/2008 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | PA, USA |
10/19/2010 |
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Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
Sponsor: | CA, USA |
10/19/2010 |
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Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
Sponsor: | CA, USA |
10/18/2007 |
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Effective Project Management for Clinical Trials
Sponsor: DIA Drug Information Association | , Spain |
10/17/2007 |
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Optimising Clinical Trial Design and Management
Sponsor: DIA Drug Information Association | , Spain |
10/17/2007 |
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Statistical Methodology in Clinical R&D
Sponsor: DIA Drug Information Association | , Spain |
10/16/2007 |
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Adverse Drug Events in Premarketing Clinical Trials and Postmarketing Pharmacovigilance: The Compliance, Medical Assessment and Risk Management Continuum
Sponsor: DIA Drug Information Association | PA, USA |
10/16/2007 |
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Computerized Systems Used in Clinical Investigations: the New FDA Guidance; An Online Course 11:00 a.m. - 12:30 p.m. (EST-New York time)
Sponsor: CFPA The Center for Professional Advancement | , |
10/16/2006 |
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Clinical Data Management
Sponsor: Drug Information Association (DIA) | PA, USA |
10/16/2006 |
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Fundamentals of Clinical Research Monitoring
Sponsor: Drug Information Association (DIA) | DC, USA |
10/16/2006 |
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Clinical Statistics for Non Statisticians
Sponsor: Drug Information Association (DIA) | , Czech Republic |
10/15/2007 |
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Multi-Track Conference: The Power of the Clinical Team
Sponsor: DIA Drug Information Association | , Spain |
10/15/2007 |
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Advanced Clinical Statistics for Non-Statisticians
Sponsor: DIA Drug Information Association | PA, USA |
10/14/2008 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | n/a, Ireland |
10/12/2011 |
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3rd Annual Partnerships in Clinical Trials Asia
Sponsor: Institute for International Research | , China |
10/12/2010 |
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Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
Sponsor: | CA, USA |
10/12/2010 |
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Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
Sponsor: | CA, USA |
10/12/2009 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation and Education | PA, USA |
10/12/2009 |
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Practical Strategies for Developing Preclinical and Phase 1 Oral Drug Formulations
Sponsor: | WI, USA |
10/09/2007 |
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Proven Strategies for Compliant Clinical Trial Results Disclosure; An Online Course 10:00AM - 11:30AM
Sponsor: DIA Drug Information Association | , |
10/09/2007 |
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Good Clinical Practices Workshop
Sponsor: QD-Quality and Training Solutions, Inc. | CA, USA |
10/09/2007 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | CA, USA |
10/09/05 |
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Society of Clinical Data Management
Sponsor: Society of Clinical Data Management | CA, USA |
10/08/2007 |
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Applied Drug Development 1: Preclinical and Drug Product Design Strategies
Sponsor: University of Wisconsin School of Pharmacy | WI, USA |
10/08/2007 |
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Excellence in Pharmacovigilance: Clinical Trials and Post marketing
Sponsor: DIA Drug Information Association | , France |
10/07/2010 |
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Integrating Clinical Evaluation and Risk Management (ISO 14971)
Sponsor: | CA, USA |
10/07/2010 |
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Integrating Clinical Evaluation and Risk Management (ISO 14971)
Sponsor: | CA, USA |
10/06/2009 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation and Education | , Ireland |
10/05/2010 |
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The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor: | CA, USA |
10/05/2010 |
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The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor: | CA, USA |
10/05/2010 |
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42nd National Congress of the Italian Society of Clinical Biochemistry and Molecular Biology (SIBioC)
Sponsor: National Congress of the Italian Society of Clinical Biochemistry and Molecular Biology (SIBioC) | , Italy |
10/05/2010 |
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The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor: | CA, USA |
10/05/2010 |
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The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor: | California, USA |
10/05/2006 |
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Overview for Regulatory Affairs Personnel on the Requirements for Submission of Clinical Data for NDAs
Sponsor: Drug Information Association (DIA) | PA, USA |
10/04/2006 |
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Statistical Methodology in Clinical R&D
Sponsor: Drug Information Association (DIA) | Baden-Wurttemberg, Germany |
10/03/2007 |
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The EU Clinical Trial Directives
Sponsor: The Center for Professional Innovation & Education | , Germany |
10/01/2007 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09-03-2005 |
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Global Clinical and Post-Marketing Surveillance
Sponsor: GTC Bio | CA, USA |
09/29/2010 |
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Ensuring GCP compliance through quality auditing in clinical trial
Sponsor: | CA, USA |
09/29/2010 |
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Ensuring GCP compliance through quality auditing in clinical trial
Sponsor: | CA, USA |
09/28/2010 |
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Clinical Applications and Workshop
Sponsor: Waters | MN, USA |
09/28/2006 |
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Harmonisation Beyond the Implementation of the Clinical Trial Directive
Sponsor: Drug Information Association (DIA) | Copenhagen, Denmark |
09/26/2006 |
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Data on Demand: The Optimization of Clinical Data Management
Sponsor: Drug Information Association (DIA) | PA, USA |
09/25/2006 |
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Introduction to Good Clinical Practices and Auditing
Sponsor: Drug Information Association (DIA) | PA, USA |
09/25/2006 |
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Bridging the Gaps between GCP, Clinical Trial Safety and Postmarketing Vigilance: Regulatory Compliance Challenges for International Pharmaceutical and Medical Device Companies
Sponsor: Drug Information Association (DIA) | DC, USA |
09/25/2006 |
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3rd Latin American Congress for Clinical Research: Advanced Topics in Clinical Research/Drug Development for Clinical Research Professionals
Sponsor: Drug Information Association (DIA) | Sao Paulo, Brazil |
09/24/2009 |
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Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation & Education | , Ireland |
09/24/2008 |
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The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/24/2007 |
|
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | , Ireland |
09/23/2008 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/22/2009 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/22/2008 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | n/a, Germany |
09/22/2008 |
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Perspectives on Good Laboratory and Manufacturing Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/22/2006 |
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Imaging in Clinical Trials: Considerations from FDA and EMEA
Sponsor: Drug Information Association (DIA) | PA, USA |
09/21/2009 |
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Good Laboratory Practices for Pre-Clinical Testing
Sponsor: The Center for Professional Innovation & Education | PA, uSA |
09/19/2011 |
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15th Annual eClinical Integration Summit
Sponsor: Institute for International Research | Masachusetts, United States |
09/19/2007 |
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Good Clinical Practices
Sponsor: The Center for Professional Innovation & Education | , Ireland |
09/18/2006 |
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Clinical Research and Drug Registration in China and India
Sponsor: Drug Information Association (DIA) | NJ, USA |
09/18/2006 |
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Clinical Statistics for Nonstatisticians
Sponsor: Drug Information Association (DIA) | MD, USA |
09/14/2009 |
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The CTD/eCTD: Building the Marketing Application throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/11/2008 |
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Understanding Regulatory & Clinical Information Systems During Product Development
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/11/2006 |
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Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: The Center for Professional Advancement (CFPA) | California, USA |
09/09/2008 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | PA, USA |
09/08/2008 |
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Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation & Education | n/a, Ireland |
09/03/2009 |
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Detecting Fraud and Misconduct in Clinical Trials
Sponsor: The Center for Professional Innovation and Education | CA, USA |
09/02/2010 |
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Vendor selection in clinical trials, assessment activities, audits and log of preferred partners
Sponsor: | CA, USA |
09/02/2010 |
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Ensuring GCP compliance through quality auditing in clinical trial
Sponsor: | CA, USA |
09/02/2010 |
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Vendor selection in clinical trials, assessment activities, audits and log of preferred partners
Sponsor: | California, USA |
09/01/2010 |
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Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
Sponsor: | CA, USA |
08/26/2010 |
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How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Sponsor: | CA, USA |
08/26/2010 |
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How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Sponsor: | California, USA |
08/24/2010 |
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Fundamentals of FDA's Clinical Trial Audits - A Must- Know for Audit preparation
Sponsor: | California, USA |
08/24/2010 |
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Fundamentals of FDA's Clinical Trial Audits - A Must- Know for Audit preparation
Sponsor: | CA, USA |
08/22/2007 |
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Good Clinical Practices
Sponsor: The Center for Professional Innovation & Education | PA, USA |
08/22/2005 |
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DIA Advanced Topics in Clinical Research/Drug Development Training Course
Sponsor: DIA | PA, USA |
08/21/2007 |
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How to Monitor Clinical Trials for Good Clinical Practice (GCP) Compliance
Sponsor: The Center for Professional Innovation & Education | PA, USA |
08/21/2006 |
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Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Infromation Association (DIA) | PA, USA |
08/13/2007 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | California, USA |
08/12/2010 |
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Outsourcing Clinical Trials in Latin America
Sponsor: | California, USA |
08/07/2007 |
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The European UnionClinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | California, USA |
08/07/2006 |
|
Fundamentals of Clinical Research Monitoring
Sponsor: Drug Information Association (DIA) | MA, USA |
08/01/2011 |
|
2nd Annual Partnerships in Clinical Trials Latin America
Sponsor: Institute for International Research | , Brazil |
07/26/2007 |
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Outsourcing Preclinical Toxicology Studies
Sponsor: The Center for Professional Innovation & Education | CA, USA |
07/25/2006 |
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The American Society for Clinical Laboratory Science (ASCLS), 2006 Annual Meeting
Sponsor: The American Society for Clinical Laboratory Science (ASCLS), | IL, USA |
07/24/2011 |
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American Association of Clinical Chemistry AACC 2011 Annual Meeting
Sponsor: American Association of Clinical Chemistry AACC | GA, USA |
07/24/2006 |
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Pediatric Clinical Research: Where Are We and Where Do We Go From Here?
Sponsor: Drug Information Association (DIA) | NC, USA |
07/23/2005 |
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XIX International Congress of Clinical Chemistry
Sponsor: CLSI | FL , USA |
07/17/2008 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | CA, USA |
07/16/2009 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | CA, USA |
07/13/2006 |
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Clinical Applications of Biomarkers
Sponsor: | Virginia, USA |
07/12/2007 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | California, USA |
07/11/2005 |
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Development Strategies and Clinical Trial Methods of Oncologic Products
Sponsor: PERI | VA, USA |
07/10/2006 |
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Development Strategies and Clinical Trial Methods for Oncologic Products
Sponsor: | Virginia, USA |
06-26-2006 |
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Institute for International Research's 2nd Annual Optimizing Preclinical Outsourcing
Sponsor: Institute for International Research (IIR) | mA, USA |
06/29/2009 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/29/2006 |
|
Clinical Statistics for Non Statisticians
Sponsor: Drug Information Association (DIA) | Amsterdam, Netherlands |
06/23/2008 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/16/2008 |
|
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/15/2009 |
|
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/15/2009 |
|
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/13/2005 |
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Clinical Development of Drugs for Asthma and COPD
Sponsor: PERI | MD, USA |
06/12/2008 |
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Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/08/2005 |
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Essential Training Course for New Clinical Statisticians
Sponsor: PERI | VA, USA |
06/04/2009 |
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Detecting Fraud and Misconduct in Clinical Trials
Sponsor: The Center for Professional Innovation & Education | PA, USA |
06/03/2008 |
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4th Annual Preclinical Outsourcing & Partnerships
Sponsor: Institute of International Research | MD, USA |
06/02/2008 |
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The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education | CA, USA |
06/01/2009 |
|
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | CA, USA |
05/27/2008 |
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The EU Clinical Trial Directive
Sponsor: Pharmaceutical | OH, USA |
05/22/2006 |
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Development of a Clinical Study Report Training Course
Sponsor: Drug Information Association (DIA) | PA, USA |
05/20/2011 |
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Last changes in Canadian ethics regulations for clinical trial
Sponsor: Compliance Online | CA, USA |
05/19/2008 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | Berlin, Germany |
05/18/2005 |
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Advanced Good Clinical Practices
Sponsor: PERI | MD, USA |
05/16/2005 |
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Introduction to Clinical Data Management
Sponsor: PERI | PA, USA |
05/15/2011 |
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21st International Congress of Clinical Chemistry and Laboratory Medicine IFCC WorldLab 2011
Sponsor: 21st International Congress of Clinical Chemistry and Laboratory Medicine | , Germany |
05/15/2008 |
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Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education | Dublin, Ireland |
05/15/2007 |
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Cambridge Healthtech Institute CHI's Global R&D Congress: Strategic Planning for Discovery, Development and Clinical Operations in China, India and other Emerging Regions
Sponsor: Cambridge Healthtech Institute (CHI) | PA, USA |
05/12/2010 |
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Data Monitoring Committees (DMCs) in Clinical Research - its effect on subject public safety and how can it be effectively set up
Sponsor: | California, USA |
05/12/2010 |
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Data Monitoring Committees (DMCs) in Clinical Research - its effect on subject public safety and how can it be effectively set up
Sponsor: | California, USA |
05/11/2009 |
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Good Laboratory Practices (GLP) for Pre-Clinical Testing
Sponsor: The Center for Professional Innovation & Education | CA, USA |
05/11/2005 |
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Effective Planning and Management of Clinical Trials: Improving the Process from Protocol to Recruitment
Sponsor: PERI | PA, USA |
05/08/2006 |
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Challenges and Practical Aspects of Assessing Clinical QT Prolongation/ Proarrhythmia Risk and Implications for the Critical Pathway
Sponsor: Drug Information Association | DC , USA |
05/08/2006 |
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Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Information Association (DIA ) | PA, USA |
05/07/2007 |
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Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Information Association (DIA) | PA, USA |
05/06/2009 |
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Introduction to Clinical Trial Management
Sponsor: The Center for Professional Innovation & Education | , Ireland |
05/03/2006 |
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Clinical Trial Delays - Assuring Predictable and Timely Completion of Patient Enrollment
Sponsor: Drug Information Association (DIA) | , |
05/02/2005 |
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Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
Sponsor: PERI | Washington DC, USA |
05/01/2008 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | PA, USA |
04/30/2009 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | , Ireland |
04/30/2006 |
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The Pan American Group for Rapid Viral Diagnosis (PAGRVD) 22nd Annual Clinical Virology Symposium
Sponsor: The Pan American Group for Rapid Viral Diagnosis (PAGRVD) | FL, USA |
04/28/2010 |
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Understanding Clinical Trials Regulations in Latin America
Sponsor: | California, USA |
04/28/2010 |
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Understanding Clinical Trials Regulations in Latin America
Sponsor: | California, USA |
04/28/2005 |
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CDC A Plan of Action: Bioterrorism Preparedness for Clinical Laboratories
Sponsor: CDC | TN, USA |
04/27/2009 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | , Germany |
04/26/2006 |
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2006 CLINICAL AND LABORATORY STANDARDS INSTITUTE LEADERSHIP CONFERENCE
Sponsor: The Clinical and Laboratory Standards Institute | VA, USA |
04/24/2006 |
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Good Clinical Practices for the Clinical Research Professional
Sponsor: Drug Information Association | Pennsylvania, USA |
04/24/2006 |
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Advanced Clinical Statistics for Nonstatisticians
Sponsor: Drug Information Association (DIA) | IL, USA |
04/21/2009 |
|
Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
Sponsor: The Center for Professional Innovation & Education | PA, USA |
04/21/2008 |
|
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | Dublin, Ireland |
04/20/2009 |
|
Applied Drug Development: Preclinical and Drug Product Design Strategies
Sponsor: | WI, USA |
04/20/2005 |
|
Inaugural Integrative Preclinical Development
Sponsor: Cambridge Healthtech Institute | CA, USA |
04/18/2005 |
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3rd World Conference on Drug Absorption, Transport and Delivery: Clinical Significance and Regulatory Impact (3rd WCDATD)
Sponsor: EUFEPS | Barcelona, Spain |
04/16/2007 |
|
Clinical Statistics for Nonstatisticians Training Course
Sponsor: Drug Information Association (DIA) | PA, USA |
04/14/2009 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | PA, USA |
04/14/2008 |
|
Pediatric Clinical Trials Symposium
Sponsor: Institute of International Research | NV, USA |
04/11/2005 |
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Biologics Drug Development: An Integrated Overview of Manufacturing, Nonclinical, Clinical and Regulatory Requirements
Sponsor: PERI | MD, USA |
04/11/11 |
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Biology and CMC Strategies in the Nonclinical Development of Pharmaceuticals
Sponsor: | WI, USA |
04/10/2006 |
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Pre-Clinical to Early Clinical Development
Sponsor: The Center for Business Intelligence | PA, USA |
04/10/2005 |
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Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
Sponsor: | Washington, DC, USA |
04/07/2008 |
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Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: CFPA The Center for Professional Advancement | , The Netherlands |
04/06/2009 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | , Ireland |
04/04/2006 |
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16th European Congress of Clinical Microbiology and Infectious Diseases (ECCMID)
Sponsor: European Congress of Clinical Microbiology and Infectious Diseases | Nice, France |
04/03/2006 |
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Fundamentals of Clinical Research Monitoring Training Course
Sponsor: Drug Information Association | PA, USA |
03/31/2011 |
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Safety Reporting in Clinical Trials: Are you Ready for the New FDA Rules?
Sponsor: Compliance Online | CA, USA |
03/30/2010 |
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The Importance of ICH Guidelines and its Role in Achieving Good Clinical Practice
Sponsor: | California, USA |
03/29/2011 |
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Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites
Sponsor: Compliance online | CA, USA |
03/29/2006 |
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Clinical Biomarker Summit
Sponsor: Cambridge Healthtech Institute | CA, USA |
03/27/2008 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/25/2009 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | , Ireland |
03/24/2005 |
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SC on Automated Verification of Clinical Lab. Test Results
Sponsor: CLSI | PA, USA |
03/23/2009 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/21/2007 to 03/23/2007 |
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Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: The Center for Professional Advancement | NJ, USA |
03/21/2007 |
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Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: Center for Professional Advancement (CFPA) | NJ, USA |
03/20/2011 |
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20th Annual Partnerships in Clinical Trials
Sponsor: | Arizona, US |
03/19/2008 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/19/2007 |
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Clinical Data Management
Sponsor: Drug Information Association (DIA) | FL, USA |
03/19/2007 |
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Clinical Biomarkers Summit
Sponsor: Cambridge Healthtech Institute | California, USA |
03/18/2007 |
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22nd Annual DRUG INFORMATION ASSOCIATION'S CLINICAL DATA MANAGEMENT Symposium and Exhibition Integration Across the Clinical Trial Continuum
Sponsor: Drug Information Association (DIA) | FL, USA |
03/16/2009 |
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Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/16/2005 |
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NCCLS 2005 Clinical and Laboratory Standards Institute Leadership Conference
Sponsor: CLIS | MD, USA |
03/14/2005 |
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Charles River EU Clinical Trials Directive Seminars Series
Sponsor: Charles River | MA, USA |
03/12/2008 |
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The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/11/2009 |
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The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/10/2009 |
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The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/10/2008 |
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Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education | PA, USA |
03/10/2008 |
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Medical Device Clinical Trials CEO Meeting
Sponsor: Q1 Productions | California, USA |
03/05/2012 |
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21st Annual Partnerships in Clinical Trials
Sponsor: Institute for International Research | FL, USA |
03/05/2011 |
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21st Annual Partnerships in Clinical Trials
Sponsor: Institute for Internatinal Research | FL, USA |
03/04/2011 |
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Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Sponsor: Compliance Online | CA, USA |
03/04/12 |
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21st Annual Partnerships in Clinical Trials
Sponsor: | FL, USA |
03/03/2008 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | PA, USA |
02/28/2007 |
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Preclinical Development
Sponsor: Cambridge Healthtech Institute | CA, USA |
02/28/2007 |
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Clinical Trials in India and Asia
Sponsor: Cambridge Healthtech Institute | CA, USA |
02/27/2008 |
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Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: CFPA The Center for Professional Advancement | NJ, USA |
02/27/2007 |
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CHI's Third Annual Biomarkers in Preclinical Development
Sponsor: BayBio | California, USA |
02/26/2007 to 02/28/2007 |
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Preparation, Packaging and Labeling of Clinical Trial Materials
Sponsor: The Center for Professional Advancement (CFPA) | , The Netherlands |
02/25/2008 |
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Clinical Trials Progress 2008
Sponsor: | FL, USA |
02/23/2006 |
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Pre-Clinical and Clinical Strategies for Pediatric Drug Development
Sponsor: The Center for Business Intelligence | VA, USA |
02/22/2007 |
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2007 Clinical Laboratory Educators' Conference
Sponsor: The American Society for Clinical Laboratory Science | KY, USA |
02/11/2008 |
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Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education | PA, Ireland |
02/09/2009 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | PA, USA |
02/09/2008 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | PA, USA |
02/08/2011 |
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Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancePanel
Sponsor: global Compliance Panel | DE, USA |
02/06/2007 |
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Development of Clinical Study Report Training Course
Sponsor: Drug Information Association (DIA) | PA, USA |
02/04/2008 |
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Introduction to Clinical Trial Management
Sponsor: The Center for Professional Innovation & Education | PA, USA |
02/03/2011 |
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Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
Sponsor: | DE, USA |
01/31/2008 |
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FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education | , Ireland |
01/31/2008 |
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11th Annual Workshop in Japan for CLINICAL DATA MANAGEMENT: HOW IMPORTANT THE
Sponsor: DIA Drug Information Association | , Japan |
01/29/2007 |
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DIA's 10th Annual Workshop in Japan for Clinical Data Management: Return to the Basics- Does Quality Meet
Sponsor: Drug Information Association (DIA) | , Japan |
01/27/2009 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | CA, USA |
01/26/2009 |
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Good Laboratory Practices for Pre-Clinical Testing
Sponsor: The Center for Professional Innovation & Education | PA, USA |
01/24/2008 |
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How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education | CA, USA |
01/24/2007 |
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Sharing Knowledge to Improve Clinical Drug Development and Regulatory Decisions: Data/models of Diseases, Drugs, Placebo, Baseline, and Dropouts
Sponsor: Drug Information Association (DIA) | DC, USA |
01/24/2007 |
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Sharing Data and Models to Improve Clinical Drug Development and Regulatory Decisions
Sponsor: Drug Information Association | DC, USA |
01/20/2006 |
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Safety Testing of Drug Metabolites: The Impact on Clinical and Toxicology Programs
Sponsor: Barnett Educational Services | , Webinar |