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Our clinical trials
Why participate?
Why take part in a clinical trial?
What is a clinical trial?
Are clinical trials safe?
What is the information from clinical trials used for?
How is information from a clinical trial kept confidential?
What is a clinical trial report?
Our commitment to transparency
Registration of clinical trials
Clinical trial reports and synopses
Technical trial results
Access to anonymised data
For researchers
Step 1: Express an interest in accessing clinical trial data
Step 2: Submit a research proposal
Step 3: Receive a decision from the review board
Step 4: Sign an agreement
Step 5: Receive the dataset
Step 6: Publish the research results
Patient and Safety Review Board
Approved research proposals and publications
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Why participate?
Why participate?
Why take part in a clinical trial?
People are free to decide if they want to take part in a trial or not. It is important that people taking part in a trial understand why the research is being done and what it will involve.
What is a clinical trial?
A clinical trial is a research study where people are invited to try a new medicine. Clinical trials test if a new medicine works and if it is safe.
Are clinical trials safe?
The safety and well-being of the people taking part are placed above all else in a clinical trial.
What is the information from clinical trials used for?
The information from clinical trials helps researchers to answer questions about medicines, diseases, or people’s health.
How is information from a clinical trial kept confidential?
During a clinical trial, personal information about the people taking part is collected.
What is a clinical trial report?
All results from a clinical trial are described in a scientific report written for researchers, health professionals, and authorities who approve medicines. This report is called a clinical trial report or clinical study report.