Good Clinical Practice (GCP) is an international standard of ethics and scientific quality for designing, conducting, recording and reporting trials involving the participation of human beings.
Conducting clinical research in Brazil generates a series of benefits, such as: access to new technologies; scientific exchange between researchers; training and qualification of human resources; job creation; investments; patient access to excellent treatments; and more accurate information about the new medicine in the local population, which facilitates decision-making by regulatory agencies regarding the safety and efficacy necessary for the product to be registered in the country.
The FDA (Food and Drug Administration) Good Clinical Practice (GCP) Guide is an international quality standard defined by the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) that governs the ethical and scientific considerations for designing, conducting, recording, and reporting trials involving human subjects.
This course will cover the main concepts of Good Clinical Practices.
Course with the quality and tradition of HCX FMUSP. Sign up!
Course details