
FDA Draft Guidance on Patient Preference Information in the TPLC: Implementation
The new article highlights the key points related to the actual implementation of the information collected from patients in the form of feedback.
The new article highlights the key points related to the actual implementation of the information collected from patients in the form of feedback.
The article provides a general overview of the regulatory framework for combination products applicable in the EU in general and in Austria specifically.
The article highlights the key points related to clinical trials and the way they should be conducted in order to ensure the accuracy and reliability of the results, as well as the safety of the patients involved.
The new article pays special attention to the prerequisites of a clinical trial, addressing the matters related to protocols and key elements thereof.
The new article outlines the key ethical and safety considerations pertaining to clinical studies.