Bio Training in Abu Dhabi

Good Clinical Practice (GCP) is a set of guidelines for clinical research done on human subjects. GCP serves as the international standard for designing, conducting, monitoring, documenting, analyzing, and reporting clinical trials. In this instructor-led, live training, participants will learn the most important guidelines and fundamental principles applied in Good Clinical Practice (GCP) for clinical trials and researches involving human subjects. This course provides an overview of the different GCP areas, but provides slightly more focus on the ICH-centric GCP for Investigational Drugs and Biologics. By the end of this training, participants will be able to:

• Understand the fundamental principles of GCP for investigational drugs and biologics as based on the International Conference on Harmonization (ICH)
• Apply the guidelines stipulated by the GCP to their clinical researches and trials

Audience

• Clinical investigators
• Clinical research professionals
• Healthcare and medical professionals
• Clinical trials support staff
• Research and development staff

Format of the course

• Part lecture, part discussion, exercises and heavy hands-on practice

This course aims to give researchers an understanding of the principles of statistical design and analysis and their relevance to research in a range of scientific disciplines. It covers some probability and statistical methods, mainly through examples. This training contains around 30% of lectures, 70% of guided quizzes and labs. In the case of closed course we can tailor the examples and materials to a specific branch (like psychology tests, public sector, biology, genetics, etc...) In the case of public courses, mixed examples are used. Though various software is used during this course (Microsoft Excel to SPSS, Statgraphics, etc...) its main focus is on understanding principles and processes guiding research, reasoning and conclusion. This course can be delivered as a blended course i.e. with homework and assignments.