GCP Training

GCP Training Web Site Design New Jersey Clinical Research Audit Training
Quality assurance of medical research is essential in the prevention of scientific misconduct and fraud that is in the forefront of the news today. When uncovered by FDA inspection or media research the effect on the research facility can be devastating. The Quality Research Training Institute trains clinical professionals in GCP compliance and monitoring
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Monday February 6, 2012

  • NEW RESEARCH MISCONDUCT FINDING: PHILIPPE BOIS
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  • Duke Scientist Suspended Over Rhodes Scholar Claims
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  • Protocols and planning key to avoiding warning letters; FDA
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  • Exculpatory Language in Informed Consent
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  • FDA News Release: Saftey Information Required
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  • FDA's HSP/BIMO Initiative Accomplishments: Update September 2010
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  • Reporting Requirements for Bioavailability and Bioequivalence Studies in Humans
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  • Reporting Information Regarding Falsification of Data
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GCP FDA IRB Training

GCP FDA IRB Training

The Clinical Research Quality Assurance Expert's Expert Sourcesm
Clinical Research Audit Training

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GCP Training Classes

Is there anything new in FDA's draft guidance: "Oversight of Clinical Investigations - A Risk-Based Approach to Monitoring"?

Phyllis Kent

 FDA has recently released draft guidance on a risk-based approach to monitoring. Initial reactions have been that this is

Clinical Research Audit Training | GCP Training | GCP FDA IRB Training

GCP Training Seminars

Regulatory requirements for GCP Training

By Phyllis B. Kent

 While most of the regulatory agencies do not specify exact requirements for GCP training, if your clinical team is not performing according to GCPs, FDA or the others can cite inadequate GCP training as an observation. Therefore,
Clinical Research Audit Training | GCP Training GCP FDA IRB Training

Clinical Research Audit Training GCP Training GCP FDA IRB Training

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