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Who should attend Criticality of Laboratory Data - including EKG - in the Drug Development Process Webinar - By Compliance Global Inc.
Pharmaceutical, Biological and Device Companies with an active pipeline of products and planning on global studies Principal Investigators and sub investigators Clinical Research Scientists (PKs, Biostatisticians) Research Managers Safety Nurses Clinical Research Associates (CRAs) Clinical Research Coordinators (CRCs) Recruiting staff QA / QC auditors and staff Study Monitors Clinical Research Data managers
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Pharmaceutical, Biological and Device Companies with an active pipeline of products and planning on global studies Principal Investigators and sub investigators Clinical Research Scientists (PKs, Biostatisticians) Research Managers Safety Nurses Clinical Research Associates (CRAs) Clinical Research Coordinators (CRCs) Recruiting staff QA / QC auditors and staff Study Monitors Clinical Research Data managers

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Seminar Summary:

Webinar on drug development process with emphasis on Adverse Events and Safety Monitoring to gain first hand understanding on the Criticality of Laboratory Data (see full course description)

 
 
 

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Training Course Syllabus:


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

Overview

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 to insure IMP safety.

Which lab values outside of the Reference range are to be reported as AE’s is always a question that must be answered and will be reviewed. The question of the relationship of lab data to “FDA Adverse Event reporting system” determination is the decision of the Investigator guided by what is in the protocol.

The section on “Safety monitoring systems” includes the array of lab tests taken at prescribed intervals adjudged to answer the safety questions. Whereas evaluation of this safety data is the Investigators responsibility, it is essential for the whole team and the sponsor to be on board with the timing and extent of this testing.

The source of lab data is also important, as for the data to be interpretable it must be accurate, reliable and repeatable. For this reason the choice of a lab following the principles of “GLP” (21 CFR 58) or, better, certified in “GCLP” is a goal to be obtained.

Why Should You Attend

Unless you have extensive experience in lab data interpretation including cardiac monitoring, an overview of how best to view safety data would be very welcome indeed.

Areas Covered in this Webinar

Usefulness of Lab Testing
The Role of the Laboratory in the AE process
What to include as AEs in the Safety Monitoring Plan in a Protocol
The Regulatory requirements of AE reporting
A review of Blood Chemistry reporting situations
A review of Hematology report issues
Other results from the Lab and how they are used
What types of studies require special attention to the Lab data
Importance of avoiding the error of non-inclusion with regards to safety testing

Learning Objectives

Demonstrate the Role of the Laboratory in the AE process
Identify the True ‘Liver Function’ tests and the ‘Liver Injury’ markers
Recognize how to interpret Hematological lab results
Describe what the Urine exam tells us
Compare Liver Injury testing with Cardiovascular / EKG testing

Who Will Benefit

Pharmaceutical, Biological and Device Companies with an active pipeline of products and planning on global studies Principal Investigators and sub investigators
Clinical Research Scientists (PKs, Biostatisticians) Research Managers
Safety Nurses
Clinical Research Associates (CRAs)
Clinical Research Coordinators (CRCs)
Recruiting staff
QA / QC auditors and staff
Study Monitors
Clinical Research Data managers

Speaker Profile

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.

Seminar Summary:

Webinar on drug development process with emphasis on Adverse Events and Safety Monitoring to gain first hand understanding on the Criticality of Laboratory Data (see full course description)

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