Safeguarding of Participants
MRHA (Medicines and Healthcare products Regulatory Agency) oversee much of the medical research in the UK.
Institutional Review Boards (IRBs) oversee the centers where research is conducted. They approve protocols to ensure that the study is ethical and the volunteer’s rights are preserved.
What Does It Entail?
Studies involving volunteers to help address various health conditions with the aim of finding treatment.
Studies are conducted with a protocol which describes what types of subjects may enter the study, schedules of tests, study drugs, the length of the study and its outcomes.
Each person participating in the study must agree to follow the protocol.
To learn how to best use the treatment in a different population, such as children, in whom the treatment was not previously tested.
Involvement Privileges
Receive admission to potentially new research study medications and help others by contributing to medical research and treatment advances for those in the future
You can also obtain medical care specifically related to the condition under study
Risks Involved
Participation is indeed time consuming and there may be side effects from the study medication
Please keep in mind that the study medication is never 100% guaranteed be effective.
Volunteers Or Clients Cost
There are financial compensation to volunteers who undertake studies.
There are no cost to volunteers that enrols into our clinical research studies. Physical examinations, medications, laboratory investigations or any other diagnostic investigations as required for the study do not incur any cost to the volunteers.
Laboratory test or other diagnostic testing as indicated volunteer education on your condition that is being studied
Financial compensation may be provided for your time and travel expenses.
