Charles H. Pierce, MD, PhD, FCP, CPI Has 25+ years experience in the Clinical Research field. He now brings the message (via webinars, lectures and seminars) of Risk Management through knowledge of GCP Regulations and Investigator Responsibility to the entire investigative team to help them understand the regulations as well as the ethics of research involving human subjects. He has been involved in developing Phase I & IIa Clinical Pharmacology Units, Investigator and staff GCP training, and medical monitoring in both drug and device studies.

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Charles H. Charles H.

Speaker: Charles H. Pierce
Duration: 90 Minutes
Product ID: 700463

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Protocol Deviations and Violations:The importance of knowing how to prevent them

With the increasing frequency of real-time FDA audits, the importance of the nature and frequency of evidence of “Not following the Protocol” has gained increasing importance. Protocol more...

Charles H. Charles H.

Speaker: Charles H. Pierce
Duration: 90 Minutes
Product ID: 700002

Purchase

Criticality of Laboratory Data - including EKG - in the Drug Development Process

With the increasing frequency of real-time FDA audits and complexity of Investigational Medicinal Products (IMP’s), the wise are paying more attention to including a full range of lab tests t more...