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Need to find FDA, GMP, ICH, GLP, NON-GLP, GCP, CLIA, UKAS, AAALAC, A2LA, DEA, or ISO contract laboratories for non-clinical, preclinical, toxicology, toxicity, product safety, analytical chemistry, microbiology, virology, clinical, immunology, oncology, neurology, nutritional, physical, biomedical, bioengineering, genomics, nanotechnology, food science, toxicogenetics, proteomics, preclinical, bioanalytical, genetics, immunology, biochemistry, sterility, biophysical, efficacy, antigenecity, bioassay, pharmacokinetics, pK, pK/PD, biomarker, pharmacogenomics, medical, biomaterials, advanced materials, testing, assays, arrays, or other research and development of your pharmaceuticals, medical devices, in-vitro diagnostics, biopharmaceuticals, biologicals, food, beverages, consumer products, cosmetics, nutraceuticals, nutritional products, animal drugs or dietary supplements to validated methods, directives, or standards such as FDA, USP, BP, IVDD, CLIA, BAM, AATCC, NCCLS, ISO, ASTM, AAMI, NF, AOAC, ICH, IP, JP ?
Find Laboratories and Contract Research Organizations !
Contract Laboratory .com
Contract Laboratory .com helps you fulfill all your bioresearch, research, experiments, developments, analysis, assays, validation, in-process, stability, quality control, and finished product testing such as pharmaceuticals testing, biopharmaceuticals testing , in-vitro diagnostics testing, medical devices testing, biotechnology testing, clinical testing, blood testing, medical testing, cosmetics testing, biologics testing, food testing, cosmetics testing, pet food testing and animal drugs testing .
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Contract Research Training Courses and Conferences
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| Increase your clinical knowledge, interact with colleagues and further your contract research career at a contract research training course or clinical conference. If you would like more information, please call us Toll Free at 1-403-770-1992 or email us |
| Contract Research Training Courses and Conferences |
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start
date
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sponsor
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contract research training courses and conferences
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location
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12/13/2007 |
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Clinical and Laboratory Genomic and Genetic Standards
Sponsor: DIA Drug Information Association | MD, 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 |
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 |
11/13/2007 |
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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 |
11/01/2007 |
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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 |
10/29/2007 |
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Outsourcing Preclinical Toxicology Studies
Sponsor: The Center for Professional Innovation & Education | PA, USA |
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 |
10/20/2008 |
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Good Clinical Practices (GCPs)
Sponsor: The Center for Professional Innovation & Education | PA, 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 |
10/09/2007 |
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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 |
10/05/2006 |
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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 |
09/28/2006 |
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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 |
09/24/2008 |
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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 |
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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 |
09/22/2008 |
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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 |
09/19/2007 |
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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 |
09/11/2008 |
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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 |
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 |
08/07/2007 |
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The European UnionClinical Trial Directive
Sponsor: The Center for Professional Innovation & Education | California, USA |
08/07/2006 |
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Fundamentals of Clinical Research Monitoring
Sponsor: Drug Information Association (DIA) | MA, USA |
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 |
07/24/2006 |
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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 |
07/13/2006 |
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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 |
06/29/2006 | | | |