Course Description:
Studies of veterinary drugs are required to be conducted under VICH Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) for approval by the various regulatory agencies. Clinical trial monitoring, quality audit procedures, collection of valid data, and conduct of both clinical trials and target animal safety studies are regulatory requirements. Additionally, the FDA inspects studies submitted for regulatory approval. Understanding core concepts of veterinary drug studies is vital for organizations and personnel involved with submitting studies to regulatory agencies.
In this 1.5 day workshop conference you will learn the concepts of VICH GCP, recognize the difference between GCP and GLP and when each is used, gain an understanding of Target Animal Safety studies, and gain tools and procedures for writing clinical trial protocols, implementing quality auditing procedures, monitoring clinical trials, and assessing data validity. Practical exercises will be used to illustrate data validity and monitoring tools. Additionally, tips for managing FDA inspections of clinical trials will be presented.
Learning Objectives:
Upon completing this course participants should:
Understand the concepts of VICH GCP
Recognize the similarities and differences between GCP and GLP and their application to trial types
Understand how GLPs can be implemented
Understand Target Animal Safety studies and the structure and requirements of margin of safety studies
Have tools to write good clinical trials protocols
Understand the differences between quality audit procedures and quality assurance procedures
Understand the concepts of clinical trial monitoring
Be able to identify the attributes of valid data and gain tools to review electronic and hard copy data to assess data integrity and fraud
Have tools to handle an FDA inspection
Note: Use coupon code 232082 and get 10% off on registration.
Studies of veterinary drugs are required to be conducted under VICH Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) for approval by the various regulatory agencies. Clinical trial monitoring, quality audit procedures, collection of valid data, and conduct of both clinical trials and target animal safety studies are regulatory requirements. Additionally, the FDA inspects studies submitted for regulatory approval. Understanding core concepts of veterinary drug studies is vital for organizations and personnel involved with submitting studies to regulatory agencies.
In this 1.5 day workshop conference you will learn the concepts of VICH GCP, recognize the difference between GCP and GLP and when each is used, gain an understanding of Target Animal Safety studies, and gain tools and procedures for writing clinical trial protocols, implementing quality auditing procedures, monitoring clinical trials, and assessing data validity. Practical exercises will be used to illustrate data validity and monitoring tools. Additionally, tips for managing FDA inspections of clinical trials will be presented.
Learning Objectives:
Upon completing this course participants should:
Understand the concepts of VICH GCP
Recognize the similarities and differences between GCP and GLP and their application to trial types
Understand how GLPs can be implemented
Understand Target Animal Safety studies and the structure and requirements of margin of safety studies
Have tools to write good clinical trials protocols
Understand the differences between quality audit procedures and quality assurance procedures
Understand the concepts of clinical trial monitoring
Be able to identify the attributes of valid data and gain tools to review electronic and hard copy data to assess data integrity and fraud
Have tools to handle an FDA inspection
Note: Use coupon code 232082 and get 10% off on registration.
