Overview:
This webinar will highlight the salient points of Good Clinical Practice and will enable the participants to understand how to implement GCP to achieve clinical trial best practices, best patient safety and/or successful FDA and international regulatory authority inspections.
Why should you Attend: At its core, Good Clinical Practice (GCP) is a set of broad regulatory requirements, standards, and recommendations that apply to thousands of highly specific tasks, processes, and roles in the conduct of clinical research. It is important to remember that much of the practical standards used in the conduct of clinical trials are "best practices" derived from regulations, guidance, and industry standards and practices and not all found in black and white in the regulations.
Given the disparity between the detailed nature of clinical trial processes and tasks and the general GCP requirements and standards under which they occur, it is not surprising that interpreting and implementing GCP standards continue to represent challenges for the pharmaceutical, biotechnology, and medical device industries.
Areas Covered in the Session:
Define Good Clinical Practice (GCP)
Outline the goals of GCP
Provide a historical perspective on GCP
Outline FDA regulations relating to GCP in medical device research
How to implement GCP
How FDA Inspects for GCP
How FDA GCP relates to international regulations
This webinar will highlight the salient points of Good Clinical Practice and will enable the participants to understand how to implement GCP to achieve clinical trial best practices, best patient safety and/or successful FDA and international regulatory authority inspections.
Why should you Attend: At its core, Good Clinical Practice (GCP) is a set of broad regulatory requirements, standards, and recommendations that apply to thousands of highly specific tasks, processes, and roles in the conduct of clinical research. It is important to remember that much of the practical standards used in the conduct of clinical trials are "best practices" derived from regulations, guidance, and industry standards and practices and not all found in black and white in the regulations.
Given the disparity between the detailed nature of clinical trial processes and tasks and the general GCP requirements and standards under which they occur, it is not surprising that interpreting and implementing GCP standards continue to represent challenges for the pharmaceutical, biotechnology, and medical device industries.
Areas Covered in the Session:
Define Good Clinical Practice (GCP)
Outline the goals of GCP
Provide a historical perspective on GCP
Outline FDA regulations relating to GCP in medical device research
How to implement GCP
How FDA Inspects for GCP
How FDA GCP relates to international regulations
Who Should Attend
- Doctors
- Nurses
- Regulatory Affairs
- Quality Assurance
- Regulatory Authority Inspectors
- Clinical Safety Personnel
- Clinical Data Management Personnel
- IT personnel working on Clinical Systems
