
Health Data and GDPR: Take Control of Your Health Data
Health is our most valuable asset and taking control of our health data can make a huge difference to our health outcomes. Learn how you can compile and securely access all your health data.
Health is our most valuable asset and taking control of our health data can make a huge difference to our health outcomes. Learn how you can compile and securely access all your health data.
Never before has a drug or vaccine been approved for use as rapidly as vaccines for Covid-19. Learn what led to the astonishing pace of progress in the development of these vaccines and how we can use this learning to accelerate the development of new drugs.
Most people aren’t aware that they can use clinical trials as a treatment option or for financial compensation, or don’t know how to get involved. Medical doctors often don’t know of all the clinical trial options available and the best way to refer patients. A new generation of online platforms is now accessible to everyone offering comprehensive clinical trial information, trial matching and access tools.
Although the specific regional requirements for a clinical trial sponsor can vary, generally, a sponsor is responsible for guaranteeing high-quality management of the trial, the sound rationale to justify the trial, the safety of the study subjects, appropriate data handing and system validation, compliance with regulations, and the contract research organisations’ duties for each of their clinical trials.
There are 13 principles of Good Clinical Practice that provides public assurance that the rights, safety and well-being of research subjects are protected and respected, in line with the principles enunciated in the Declaration of Helsinki and other internationally recognized ethical guidelines. It also ensures the integrity of research data.
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