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Clinical Trial Training Courses and Conferences

Increase your clinical trial knowledge, interact with colleagues and further your clinical career at a clinical training training course or clinical trial conference. If you would like more information, please call us Toll Free at 1-403-770-1992 or email us
Clinical Trial Training Courses and Conferences
start date
sponsor
clinical trial training courses and conferences
location
Thursday, December 1, 2011
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
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
The Importance of ICH Guidelines and its Role in Achieving Good Clinical Practice
Sponsor:
California, United State Of America
3/3/2010
Decoding CLIA (Clinical Laboratory Improvement Amendments) Regulations: Calibration, Calibration Verification and Method Validation
Sponsor:
California, United State Of America
3/24/2010
How to Create and Understand A Statistical Analysis Plan for A Clinical Study
Sponsor:
California, United State Of America
3/17/2010
Evaluating Clinical Sites: going beyond regulatory requirements to ensure success
Sponsor:
California, United State Of America
3/10/2010
Mastering the Art of Clinical Monitoring with Enhanced Techniques - Getting Beyond the Basics
Sponsor:
California, United State Of America
12/14/2010
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
Clinical and Laboratory Genomic and Genetic Standards
Clinical and Laboratory Genomic and Genetic Standards
Sponsor: DIA Drug Information Association
MD, USA
12/10/2010
CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment - Laboratory Webinar By ComplianceOnline
Sponsor:
CA, USA
12/10/2010
How to investigate environmental monitoring excursion limits - Clinical Webinar By ComplianceOnline
Sponsor:
CA, USA
12/10/2007
Laboratory Analysis in Clinical Trials
Laboratory Analysis in Clinical Trials
Sponsor: CFPA The Center for Professional Advancement
, The Netherlands
12/10/2007
Good Clinical Practices
Good Clinical Practices
Sponsor: The Center for Professional Innovation & Education
PA, USA
12/05/2007
Pharmacokinetics and Pharmacodynamics: Principles and Applications in Pre-Clinical Drug Development
Pharmacokinetics and Pharmacodynamics: Principles and Applications in Pre-Clinical Drug Development
Sponsor: American Chemical Society
CA, USA
12/05/2006
The Quest to Enable the Electronic Clinical Trial: Finding Clarity in a Confusing World
The Quest to Enable the Electronic Clinical Trial: Finding Clarity in a Confusing World
Sponsor: Drug Information Association (DIA)
MD, USA
12/04/2006
Advanced Topics in Clinical Research/Drug Development
Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Information Association (DIA)
AZ, USA
12/04/2006
Identifying and Validating Metabolic Markers for Drug Development and Clinical Studies
Identifying and Validating Metabolic Markers for Drug Development and Clinical Studies
Sponsor: Cambridge Healthtech Institute
FL, USA
12/03/2010
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Clinical Webinar By ComplianceOnline
Sponsor:
CA, USA
12/02/2009
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation and Education
CA, USA
11/30/2010
Ethics, Standards and Identifying Risks in Clinical Research - Clinical Webinar By ComplianceOnline
Sponsor:
CA, USA
11/30/2009
Clinical Trials Design for Medical Devices
Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation and Education
CA, USA
11/27/2007
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
PA, USA
11/27/2006
Auditing and Inspecting Preclinical Research for GLP Compliance
Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: The Center for Professional Advancement (CfPA)
amsterdam, the netherlands
11/27/2006
Auditing and Inspecting Preclinical Research for GLP Compliance
Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: The Center for Professional Advancement (CfPA)
amsterdam, the netherlands
11/27/2006
Pharmacovigilance Training: Clinical Trials and Marketed Products
Pharmacovigilance Training: Clinical Trials and Marketed Products
Sponsor: Drug Information Association (DIA)
, France
11/21/2007
Auditing and Inspecting Preclinical Research for GLP Compliance
Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: CFPA The Center for Professional Advancement
, The Netherlands
11/18/2007
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
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
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation and Education
PA, USA
11/15/2011
Biomarker Application for Improved Clinical Trial Outcomes
Sponsor:
MA, USA
11/13/2007
Winning Strategies for Achieving a Quality EDC Clinical Trial Process - Sponsor/CRO, Investigator, IRB Approver and IT/IS
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
Clinical Trial Disclosure learning the landscape and reading the roadmap
Clinical Trial Disclosure learning the landscape and reading the roadmap
Sponsor: DIA Drug Information Association
FL, USA
11/12/2007
Regulatory Affairs in Medical Device Clinical Trials
Regulatory Affairs in Medical Device Clinical Trials
Sponsor: Q1 Productions.com
Az, USA
11/12/07
Good Laboratory Practices for Pre-Clinical Testing, Compliance, QA & Audit
Good Laboratory Practices for Pre-Clinical Testing, Compliance, QA & Audit
Sponsor: The Center for Professional Innovation & Education
PA, USA
11/07/2006
Beyond 2006 - Software and Services Trends for eClinical Trials
Beyond 2006 - Software and Services Trends for eClinical Trials
Sponsor: Drug Information Association (DIA)
PA, USA
11/05/2007
Early Stage Clinical Development
Early Stage Clinical Development
Sponsor: CFPA The Center for Professional Advancement
, The Netherlands
11/05/2007
Clinical Statistics for NonStatisticians
Clinical Statistics for NonStatisticians
Sponsor: DIA Drug Information Association
, Ireland
11/05/2006
The Changing World of Clinical Trials - European Clinical Research Conference, European eClinical Conference, 16th Annual European CDM Conference
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
DIA Multi-Track Conference on CDM, eClinical & Clinical Research
DIA Multi-Track Conference on CDM, eClinical & Clinical Research
Sponsor: Drug Information Association (DIA)
Basel, Switzerland
11/02/2009
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation and Education
PA, USA
11/01/2007
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
PA, USA
11/01/2006
Innovation and Reform in Clinical Trials
Innovation and Reform in Clinical Trials
Sponsor: Cambridge Health Institute
Ontario, Canada
10/30/2006
Development of a Clinical Study Report
Development of a Clinical Study Report
Sponsor: Drug Information Association (DIA)
PA, USA
10/29/2009
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation and Education
PA, USA
10/29/2007
Outsourcing Preclinical Toxicology Studies
Outsourcing Preclinical Toxicology Studies
Sponsor: The Center for Professional Innovation & Education
PA, USA
10/26/2010
6th Annual Future of Clinical Trials
Sponsor:
Vienna,
10/24/2006
Preclinical Disease Model
Preclinical Disease Model
Sponsor: Cambridge Health Institute
MA, USA
10/23/2006
Advanced Clinical Statistics for Nonstatisticians
Advanced Clinical Statistics for Nonstatisticians
Sponsor: Drug Information Association (DIA)
PA, USA
10/22/2009
Understanding Regulatory & Clinical Information Systems During Product Development
Understanding Regulatory & Clinical Information Systems During Product Development
Sponsor: The Center for Professional Innovation and Education
PA, USA
10/20/2008
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
PA, USA
10/19/2010
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
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
Effective Project Management for Clinical Trials
Effective Project Management for Clinical Trials
Sponsor: DIA Drug Information Association
, Spain
10/17/2007
Optimising Clinical Trial Design and Management
Optimising Clinical Trial Design and Management
Sponsor: DIA Drug Information Association
, Spain
10/17/2007
Statistical Methodology in Clinical R&D
Statistical Methodology in Clinical R&D
Sponsor: DIA Drug Information Association
, Spain
10/16/2007
Adverse Drug Events in Premarketing Clinical Trials and Postmarketing Pharmacovigilance: The Compliance, Medical Assessment and Risk Management Continuum
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
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)
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
Clinical Data Management
Clinical Data Management
Sponsor: Drug Information Association (DIA)
PA, USA
10/16/2006
Fundamentals of Clinical Research Monitoring
Fundamentals of Clinical Research Monitoring
Sponsor: Drug Information Association (DIA)
DC, USA
10/16/2006
Clinical Statistics for Non Statisticians
Clinical Statistics for Non Statisticians
Sponsor: Drug Information Association (DIA)
, Czech Republic
10/15/2007
Multi-Track Conference: The Power of the Clinical Team
Multi-Track Conference: The Power of the Clinical Team
Sponsor: DIA Drug Information Association
, Spain
10/15/2007
Advanced Clinical Statistics for Non-Statisticians
Advanced Clinical Statistics for Non-Statisticians
Sponsor: DIA Drug Information Association
PA, USA
10/14/2008
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
n/a, Ireland
10/12/2011
3rd Annual Partnerships in Clinical Trials Asia
Sponsor: Institute for International Research
, China
10/12/2010
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
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
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation and Education
PA, USA
10/12/2009
Practical Strategies for Developing Preclinical and Phase 1 Oral Drug Formulations
Practical Strategies for Developing Preclinical and Phase 1 Oral Drug Formulations
Sponsor:
WI, USA
10/09/2007
Proven Strategies for Compliant Clinical Trial Results Disclosure; An Online Course 10:00AM - 11:30AM
Proven Strategies for Compliant Clinical Trial Results Disclosure; An Online Course 10:00AM - 11:30AM
Sponsor: DIA Drug Information Association
,
10/09/2007
Good Clinical Practices Workshop
Good Clinical Practices Workshop
Sponsor: QD-Quality and Training Solutions, Inc.
CA, USA
10/09/2007
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
CA, USA
10/09/05
Society of Clinical Data Management
Sponsor: Society of Clinical Data Management
CA, USA
10/08/2007
Applied Drug Development 1: Preclinical and Drug Product Design Strategies
Applied Drug Development 1: Preclinical and Drug Product Design Strategies
Sponsor: University of Wisconsin School of Pharmacy
WI, USA
10/08/2007
Excellence in Pharmacovigilance: Clinical Trials and Post marketing
Excellence in Pharmacovigilance: Clinical Trials and Post marketing
Sponsor: DIA Drug Information Association
, France
10/07/2010
Integrating Clinical Evaluation and Risk Management (ISO 14971)
Sponsor:
CA, USA
10/07/2010
Integrating Clinical Evaluation and Risk Management (ISO 14971)
Sponsor:
CA, USA
10/06/2009
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation and Education
, Ireland
10/05/2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor:
CA, USA
10/05/2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor:
CA, USA
10/05/2010
 42nd National Congress of the Italian Society of Clinical Biochemistry and Molecular Biology (SIBioC)
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
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor:
CA, USA
10/05/2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Sponsor:
California, USA
10/05/2006
Overview for Regulatory Affairs Personnel on the Requirements for Submission of Clinical Data for NDAs
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
Statistical Methodology in Clinical R&D
Statistical Methodology in Clinical R&D
Sponsor: Drug Information Association (DIA)
Baden-Wurttemberg, Germany
10/03/2007
The EU Clinical Trial Directives
The EU Clinical Trial Directives
Sponsor: The Center for Professional Innovation & Education
, Germany
10/01/2007
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education
PA, USA
09-03-2005
Global Clinical and Post-Marketing Surveillance
Global Clinical and Post-Marketing Surveillance
Sponsor: GTC Bio
CA, USA
09/29/2010
Ensuring GCP compliance through quality auditing in clinical trial
Sponsor:
CA, USA
09/29/2010
Ensuring GCP compliance through quality auditing in clinical trial
Sponsor:
CA, USA
09/28/2010
Clinical Applications and Workshop
Clinical Applications and Workshop
Sponsor: Waters
MN, USA
09/28/2006
Harmonisation Beyond the Implementation of the Clinical Trial Directive
Harmonisation Beyond the Implementation of the Clinical Trial Directive
Sponsor: Drug Information Association (DIA)
Copenhagen, Denmark
09/26/2006
Data on Demand: The Optimization of Clinical Data Management
Data on Demand: The Optimization of Clinical Data Management
Sponsor: Drug Information Association (DIA)
PA, USA
09/25/2006
Introduction to Good Clinical Practices and Auditing
Introduction to Good Clinical Practices and Auditing
Sponsor: Drug Information Association (DIA)
PA, USA
09/25/2006
Bridging the Gaps between GCP, Clinical Trial Safety and Postmarketing Vigilance: Regulatory Compliance Challenges for International Pharmaceutical and Medical Device Companies
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
3rd Latin American Congress for Clinical Research: Advanced Topics in Clinical Research/Drug Development for Clinical Research Professionals
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
Clinical Trials Design for Medical Devices
Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation & Education
, Ireland
09/24/2008
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
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
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
, Ireland
09/23/2008
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
PA, USA
09/22/2009
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
PA, USA
09/22/2008
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
n/a, Germany
09/22/2008
Perspectives on Good Laboratory and Manufacturing Practices for Pre-Clinical Testing:  Compliance, QA and Audit
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
Imaging in Clinical Trials: Considerations from FDA and EMEA
Imaging in Clinical Trials: Considerations from FDA and EMEA
Sponsor: Drug Information Association (DIA)
PA, USA
09/21/2009
Good Laboratory Practices for Pre-Clinical Testing
Good Laboratory Practices for Pre-Clinical Testing
Sponsor: The Center for Professional Innovation & Education
PA, uSA
09/19/2011
15th Annual eClinical Integration Summit
Sponsor: Institute for International Research
Masachusetts, United States
09/19/2007
Good Clinical Practices
Good Clinical Practices
Sponsor: The Center for Professional Innovation & Education
, Ireland
09/18/2006
Clinical Research and Drug Registration in China and India
Clinical Research and Drug Registration in China and India
Sponsor: Drug Information Association (DIA)
NJ, USA
09/18/2006
Clinical Statistics for Nonstatisticians
Clinical Statistics for Nonstatisticians
Sponsor: Drug Information Association (DIA)
MD, USA
09/14/2009
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education
PA, USA
09/11/2008
Understanding Regulatory & Clinical Information Systems During Product Development
Understanding Regulatory & Clinical Information Systems During Product Development
Sponsor: The Center for Professional Innovation & Education
PA, USA
09/11/2006
Non-Clinical Drug Safety Evaluation and Drug Development
Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: The Center for Professional Advancement (CFPA)
California, USA
09/09/2008
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
PA, USA
09/08/2008
Clinical Trials Design for Medical Devices
Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation & Education
n/a, Ireland
09/03/2009
Detecting Fraud and Misconduct in Clinical Trials
Detecting Fraud and Misconduct in Clinical Trials
Sponsor: The Center for Professional Innovation and Education
CA, USA
09/02/2010
Vendor selection in clinical trials, assessment activities, audits and log of preferred partners
Sponsor:
CA, USA
09/02/2010
Ensuring GCP compliance through quality auditing in clinical trial
Sponsor:
CA, USA
09/02/2010
Vendor selection in clinical trials, assessment activities, audits and log of preferred partners
Sponsor:
California, USA
09/01/2010
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
How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Sponsor:
CA, USA
08/26/2010
How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Sponsor:
California, USA
08/24/2010
Fundamentals of FDA's Clinical Trial Audits - A Must- Know for Audit preparation
Sponsor:
California, USA
08/24/2010
Fundamentals of FDA's Clinical Trial Audits - A Must- Know for Audit preparation
Sponsor:
CA, USA
08/22/2007
Good  Clinical Practices
Good Clinical Practices
Sponsor: The Center for Professional Innovation & Education
PA, USA
08/22/2005
DIA Advanced Topics in Clinical Research/Drug Development Training Course
Sponsor: DIA
PA, USA
08/21/2007
How to Monitor Clinical Trials for Good Clinical Practice (GCP) Compliance
How to Monitor Clinical Trials for Good Clinical Practice (GCP) Compliance
Sponsor: The Center for Professional Innovation & Education
PA, USA
08/21/2006
Advanced Topics in Clinical Research/Drug Development
Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Infromation Association (DIA)
PA, USA
08/13/2007
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education
California, USA
08/12/2010
Outsourcing Clinical Trials in Latin America
Sponsor:
California, USA
08/07/2007
The European UnionClinical Trial Directive
The European UnionClinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
California, USA
08/07/2006
Fundamentals of Clinical Research Monitoring
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
Outsourcing Preclinical Toxicology Studies
Outsourcing Preclinical Toxicology Studies
Sponsor: The Center for Professional Innovation & Education
CA, USA
07/25/2006
The American Society for Clinical Laboratory Science (ASCLS),  2006 Annual Meeting
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
American Association of Clinical Chemistry AACC 2011 Annual Meeting
American Association of Clinical Chemistry AACC 2011 Annual Meeting
Sponsor: American Association of Clinical Chemistry AACC
GA, USA
07/24/2006
Pediatric Clinical Research: Where Are We and Where Do We Go From Here?
Pediatric Clinical Research: Where Are We and Where Do We Go From Here?
Sponsor: Drug Information Association (DIA)
NC, USA
07/23/2005
XIX International Congress of Clinical Chemistry
Sponsor: CLSI
FL , USA
07/17/2008
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
CA, USA
07/16/2009
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
CA, USA
07/13/2006
Clinical Applications of Biomarkers
Clinical Applications of Biomarkers
Sponsor:
Virginia, USA
07/12/2007
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
California, USA
07/11/2005
Development Strategies and Clinical Trial Methods of Oncologic Products
Development Strategies and Clinical Trial Methods of Oncologic Products
Sponsor: PERI
VA, USA
07/10/2006
Development Strategies and Clinical Trial Methods for Oncologic Products
Development Strategies and Clinical Trial Methods for Oncologic Products
Sponsor:
Virginia, USA
06-26-2006
Institute for International Research's 2nd Annual  Optimizing Preclinical Outsourcing
Institute for International Research's 2nd Annual Optimizing Preclinical Outsourcing
Sponsor: Institute for International Research (IIR)
mA, USA
06/29/2009
Project Management for Phase 1 & 2 Clinical Trials
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
Clinical Statistics for Non Statisticians
Sponsor: Drug Information Association (DIA)
Amsterdam, Netherlands
06/23/2008
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education
CA, USA
06/16/2008
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
CA, USA
06/15/2009
FDA Inspections of Clinical Data Systems
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
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education
CA, USA
06/13/2005
Clinical Development of Drugs for Asthma and COPD
Clinical Development of Drugs for Asthma and COPD
Sponsor: PERI
MD, USA
06/12/2008
Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education
CA, USA
06/08/2005
Essential Training Course for New Clinical Statisticians
Essential Training Course for New Clinical Statisticians
Sponsor: PERI
VA, USA
06/04/2009
Detecting Fraud and Misconduct in Clinical Trials
Detecting Fraud and Misconduct in Clinical Trials
Sponsor: The Center for Professional Innovation & Education
PA, USA
06/03/2008
4th Annual Preclinical Outsourcing & Partnerships
4th Annual Preclinical Outsourcing & Partnerships
Sponsor: Institute of International Research
MD, USA
06/02/2008
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
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)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
CA, USA
05/27/2008
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: Pharmaceutical
OH, USA
05/22/2006
Development of a Clinical Study Report Training Course
Development of a Clinical Study Report Training Course
Sponsor: Drug Information Association (DIA)
PA, USA
05/20/2011
Last changes in Canadian ethics regulations for clinical trial
Last changes in Canadian ethics regulations for clinical trial
Sponsor: Compliance Online
CA, USA
05/19/2008
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
Berlin, Germany
05/18/2005
Advanced Good Clinical Practices
Advanced Good Clinical Practices
Sponsor: PERI
MD, USA
05/16/2005
Introduction to Clinical Data Management
Introduction to Clinical Data Management
Sponsor: PERI
PA, USA
05/15/2011
21st International Congress of Clinical Chemistry and Laboratory Medicine  IFCC WorldLab 2011
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
Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education
Dublin, Ireland
05/15/2007
Cambridge Healthtech Institute CHI's Global R&D Congress: Strategic Planning for Discovery, Development and Clinical Operations in China, India and other Emerging Regions
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
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
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
Good Laboratory Practices (GLP) for Pre-Clinical Testing
Good Laboratory Practices (GLP) for Pre-Clinical Testing
Sponsor: The Center for Professional Innovation & Education
CA, USA
05/11/2005
Effective Planning and Management of Clinical Trials: Improving the Process from Protocol to Recruitment
Effective Planning and Management of Clinical Trials: Improving the Process from Protocol to Recruitment
Sponsor: PERI
PA, USA
05/08/2006
Challenges and Practical Aspects of Assessing Clinical QT Prolongation/   Proarrhythmia Risk and Implications for the Critical Pathway
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
Advanced Topics in Clinical Research/Drug Development
Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Information Association (DIA )
PA, USA
05/07/2007
Advanced Topics in Clinical Research/Drug Development
Advanced Topics in Clinical Research/Drug Development
Sponsor: Drug Information Association (DIA)
PA, USA
05/06/2009
Introduction to Clinical Trial Management
Introduction to Clinical Trial Management
Sponsor: The Center for Professional Innovation & Education
, Ireland
05/03/2006
Clinical Trial Delays - Assuring Predictable and Timely Completion of Patient Enrollment
Clinical Trial Delays - Assuring Predictable and Timely Completion of Patient Enrollment
Sponsor: Drug Information Association (DIA)
,
05/02/2005
Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
Sponsor: PERI
Washington DC, USA
05/01/2008
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
PA, USA
04/30/2009
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
, Ireland
04/30/2006
The Pan American Group for Rapid Viral Diagnosis (PAGRVD) 22nd Annual Clinical Virology Symposium
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
Understanding Clinical Trials Regulations in Latin America
Sponsor:
California, USA
04/28/2010
Understanding Clinical Trials Regulations in Latin America
Sponsor:
California, USA
04/28/2005
CDC A Plan of Action: Bioterrorism Preparedness for Clinical Laboratories
Sponsor: CDC
TN, USA
04/27/2009
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
, Germany
04/26/2006
2006 CLINICAL AND LABORATORY STANDARDS INSTITUTE LEADERSHIP CONFERENCE
Sponsor: The Clinical and Laboratory Standards Institute
VA, USA
04/24/2006
Good Clinical Practices for the Clinical Research Professional
Good Clinical Practices for the Clinical Research Professional
Sponsor: Drug Information Association
Pennsylvania, USA
04/24/2006
Advanced Clinical Statistics for Nonstatisticians
Advanced Clinical Statistics for Nonstatisticians
Sponsor: Drug Information Association (DIA)
IL, USA
04/21/2009
Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
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
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
Applied Drug Development: Preclinical and Drug Product Design Strategies
Sponsor:
WI, USA
04/20/2005
Inaugural  Integrative Preclinical Development
Inaugural Integrative Preclinical Development
Sponsor: Cambridge Healthtech Institute
CA, USA
04/18/2005
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
Clinical Statistics for Nonstatisticians Training Course
Sponsor: Drug Information Association (DIA)
PA, USA
04/14/2009
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
PA, USA
04/14/2008
Pediatric Clinical Trials Symposium
Pediatric Clinical Trials Symposium
Sponsor: Institute of International Research
NV, USA
04/11/2005
Biologics Drug Development: An Integrated Overview of Manufacturing, Nonclinical, Clinical and Regulatory Requirements
Biologics Drug Development: An Integrated Overview of Manufacturing, Nonclinical, Clinical and Regulatory Requirements
Sponsor: PERI
MD, USA
04/11/11
Biology and CMC Strategies in the Nonclinical Development of Pharmaceuticals
Sponsor:
WI, USA
04/10/2006
Pre-Clinical to Early Clinical Development
Pre-Clinical to Early Clinical Development
Sponsor: The Center for Business Intelligence
PA, USA
04/10/2005
Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
Sponsor:
Washington, DC, USA
04/07/2008
Non-Clinical Drug Safety Evaluation and Drug Development
Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: CFPA The Center for Professional Advancement
, The Netherlands
04/06/2009
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education
, Ireland
04/04/2006
16th European Congress of Clinical Microbiology and Infectious Diseases (ECCMID)
Sponsor: European Congress of Clinical Microbiology and Infectious Diseases
Nice, France
04/03/2006
Fundamentals of Clinical Research Monitoring Training Course
Fundamentals of Clinical Research Monitoring Training Course
Sponsor: Drug Information Association
PA, USA
03/31/2011
Safety Reporting in Clinical Trials: Are you Ready for the New FDA Rules?
Safety Reporting in Clinical Trials: Are you Ready for the New FDA Rules?
Sponsor: Compliance Online
CA, USA
03/30/2010
The Importance of ICH Guidelines and its Role in Achieving Good Clinical Practice
Sponsor:
California, USA
03/29/2011
Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites
Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites
Sponsor: Compliance online
CA, USA
03/29/2006
Clinical Biomarker Summit
Clinical Biomarker Summit
Sponsor: Cambridge Healthtech Institute
CA, USA
03/27/2008
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/25/2009
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
, Ireland
03/24/2005
SC on Automated Verification of Clinical Lab. Test Results
Sponsor: CLSI
PA, USA
03/23/2009
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/21/2007 to 03/23/2007
Non-Clinical Drug Safety Evaluation and Drug Development
Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: The Center for Professional Advancement
NJ, USA
03/21/2007
Non-Clinical Drug Safety Evaluation and Drug Development
Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: Center for Professional Advancement (CFPA)
NJ, USA
03/20/2011
20th Annual Partnerships in Clinical Trials
Sponsor:
Arizona, US
03/19/2008
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/19/2007
Clinical Data Management
Clinical Data Management
Sponsor: Drug Information Association (DIA)
FL, USA
03/19/2007
Clinical Biomarkers Summit
Clinical Biomarkers Summit
Sponsor: Cambridge Healthtech Institute
California, USA
03/18/2007
22nd Annual DRUG INFORMATION ASSOCIATION'S CLINICAL DATA MANAGEMENT Symposium and Exhibition Integration Across the Clinical Trial Continuum
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
Clinical Trials Design for Medical Devices
Clinical Trials Design for Medical Devices
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/16/2005
NCCLS 2005 Clinical and Laboratory Standards Institute Leadership Conference
Sponsor: CLIS
MD, USA
03/14/2005
Charles River EU Clinical Trials Directive Seminars Series
Charles River EU Clinical Trials Directive Seminars Series
Sponsor: Charles River
MA, USA
03/12/2008
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/11/2009
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
The CTD/eCTD: Building the Marketing Application Throughout Clinical Development
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/10/2009
The EU Clinical Trial Directive
The EU Clinical Trial Directive
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/10/2008
Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Good Laboratory Practices for Pre-Clinical Testing: Compliance, QA and Audit
Sponsor: The Center for Professional Innovation & Education
PA, USA
03/10/2008
Medical Device Clinical Trials CEO Meeting
Medical Device Clinical Trials CEO Meeting
Sponsor: Q1 Productions
California, USA
03/05/2012
21st Annual Partnerships in Clinical Trials
Sponsor: Institute for International Research
FL, USA
03/05/2011
21st Annual Partnerships in Clinical Trials
Sponsor: Institute for Internatinal Research
FL, USA
03/04/2011
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Sponsor: Compliance Online
CA, USA
03/04/12
21st Annual Partnerships in Clinical Trials
Sponsor:
FL, USA
03/03/2008
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
PA, USA
02/28/2007
Preclinical Development
Preclinical Development
Sponsor: Cambridge Healthtech Institute
CA, USA
02/28/2007
Clinical Trials in India and Asia
Clinical Trials in India and Asia
Sponsor: Cambridge Healthtech Institute
CA, USA
02/27/2008
Non-Clinical Drug Safety Evaluation and Drug Development
Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: CFPA The Center for Professional Advancement
NJ, USA
02/27/2007
CHI's Third Annual Biomarkers in Preclinical Development
CHI's Third Annual Biomarkers in Preclinical Development
Sponsor: BayBio
California, USA
02/26/2007 to 02/28/2007
Preparation, Packaging and Labeling of Clinical Trial Materials
Preparation, Packaging and Labeling of Clinical Trial Materials
Sponsor: The Center for Professional Advancement (CFPA)
, The Netherlands
02/25/2008
Clinical Trials Progress 2008
Clinical Trials Progress 2008
Sponsor:
FL, USA
02/23/2006
Pre-Clinical and Clinical Strategies for Pediatric Drug Development
Pre-Clinical and Clinical Strategies for Pediatric Drug Development
Sponsor: The Center for Business Intelligence
VA, USA
02/22/2007
2007 Clinical Laboratory Educators' Conference
2007 Clinical Laboratory Educators' Conference
Sponsor: The American Society for Clinical Laboratory Science
KY, USA
02/11/2008
Project Management for Phase 1 & 2 Clinical Trials
Project Management for Phase 1 & 2 Clinical Trials
Sponsor: The Center for Professional Innovation & Education
PA, Ireland
02/09/2009
Good Clinical Practices (GCPs)
Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education
PA, USA
02/09/2008
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
PA, USA
02/08/2011
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancePanel
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancePanel
Sponsor: global Compliance Panel
DE, USA
02/06/2007
Development of Clinical Study Report Training Course
Development of Clinical Study Report Training Course
Sponsor: Drug Information Association (DIA)
PA, USA
02/04/2008
Introduction to Clinical Trial Management
Introduction to Clinical Trial Management
Sponsor: The Center for Professional Innovation & Education
PA, USA
02/03/2011
Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
Sponsor:
DE, USA
01/31/2008
FDA Inspections of Clinical Data Systems
FDA Inspections of Clinical Data Systems
Sponsor: The Center for Professional Innovation & Education
, Ireland
01/31/2008
11th Annual Workshop in Japan for CLINICAL DATA MANAGEMENT: HOW IMPORTANT THE
11th Annual Workshop in Japan for CLINICAL DATA MANAGEMENT: HOW IMPORTANT THE
Sponsor: DIA Drug Information Association
, Japan
01/29/2007
DIA's 10th Annual Workshop in Japan for Clinical Data Management: Return to the Basics- Does Quality Meet
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
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
CA, USA
01/26/2009
Good Laboratory Practices for Pre-Clinical Testing
Good Laboratory Practices for Pre-Clinical Testing
Sponsor: The Center for Professional Innovation & Education
PA, USA
01/24/2008
How to Monitor Clinical Trials for GCP Compliance
How to Monitor Clinical Trials for GCP Compliance
Sponsor: The Center for Professional Innovation & Education
CA, USA
01/24/2007
Sharing Knowledge to Improve Clinical Drug Development and Regulatory Decisions: Data/models of Diseases, Drugs, Placebo, Baseline, and Dropouts
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
Sharing Data and Models to Improve Clinical Drug Development and Regulatory Decisions
Sharing Data and Models to Improve Clinical Drug Development and Regulatory Decisions
Sponsor: Drug Information Association
DC, USA
01/20/2006
Safety Testing of Drug Metabolites: The Impact on Clinical and Toxicology Programs
Safety Testing of Drug Metabolites: The Impact on Clinical and Toxicology Programs
Sponsor: Barnett Educational Services
, Webinar
>

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