Research practices

Investment in R&D is at the core of our business and we make sure we carry out our research to high ethical and quality standards in all the countries in which we operate. Whether it’s a patient’s safety during a clinical trial or the necessary use of an animal in our research, we always apply recognised standards and principles of good medical science, integrity and ethics.

We aim to address any concerns by being open about our research and regularly engaging with academic scientists, regulators, policymakers and other stakeholders.

Transparency of our research

We are committed to reporting the results of clinical research into our medicines and vaccines, whether the outcomes are positive or negative. We do this by:

  • posting the results of our research on our publicly accessible Clinical Study Register website
  • seeking to publish all research results as full papers in peer-reviewed scientific journals
  • enabling researchers to access detailed anonymised patient-level data from trials
  • expanding the information made publically available on our Clinical Study Register

The Clinical Study Register - which receives on average over 14,000 visits each month - now includes more than 5,400 summaries of trial results, which are posted regardless of whether the outcomes might be considered positive or negative. In 2013, we expanded this to include Clinical Study Reports (CSRs) – formal study reports on the design, methods and results of clinical trials which form the basis of submissions to regulatory agencies.

Sharing our research

In addition, we are being more open with our expertise and know-how and around research into neglected tropical diseases, and loking to share our intellectual property where appropriate to further innovation targeting diseases of the developing world.