69.00€
During the course “Introduction to Good Clinical Practice” you will learn basic information related to GCP. Wondering what rules to follow when conducting a Clinical Trial? Not sure on what basis they were even established?
During this course, we will discuss the historical basis for the creation of the Good Clinical Practice recommendations. We’ll tell you why it’s so important to take an ethical approach to conduct research and the consequences of trivializing this issue. We will also discuss all 13 principles that the GCP recommendations state should be followed when conducting clinical trials.
Unsure what the difference is between the responsibilities of the Sponsor and the Investigator in conducting a clinical trial? And what does the Bioethics Committee do? We will also discuss these issues in the basic courses in Good Clinical Practice knowledge.
Want to make sure you’re following the most important recommendations for the clinical trial industry? Do you want to be sure that your study is conducted in accordance with them?
If so, this course is for you!
She has been involved in the clinical research industry since 2015. She currently works for a global pharmaceutical company as a Manager in the Clinical Documentation team, where her main role is FSO Operations Lead.
She places high value on personal development and the quality of performed activities, which makes her a valued member of project teams. She has operational experience gained in global CROs and pharmaceutical companies. She has worked on both investigational and medical device projects in a variety of therapeutic areas.
From the very beginning of her work in clinical research, she has struggled with the complex nature of clinical trial documentation and TMF, which she continues to explore to this day.
In addition to her day job, she is actively involved in the academic community, initially as a coordinator and support to the manager of a post-graduate study in the clinical trial area. Currently, she is a lecturer at Conducting and Monitoring Clinical Trials and a manager of postgraduate study Project Management in Clinical Trials.
This collaboration started after the previously completed postgraduate studies in Conducting and Monitoring Clinical Trials. Graduate of Nicolaus Copernicus University in Torun in the faculties of molecular biology and environmental protection.
Although she started her professional life at the Central Forensic Laboratory of the Police, she now finds herself perfectly at work in clinical project activities and now she is conducting other types of investigations.
Don’t miss out on this opportunity to revolutionize your employee development process with AIDIFY’s freemium license. Fill out our form to get started today!
Reviews
There are no reviews yet.