We facilitate the discovery and development of cutting-edge treatments by running high-quality, ethical clinical trials.
We prioritise participant safety, education, and transparency – ensuring each person understands their role and rights throughout the study.
We provide reliable, fast, and compliant clinical trial operations supported by highly experienced
investigators and staff.
Coming Soon
We are currently enrolling participants for a range of active clinical studies. These trials explore new treatments, therapies, and diagnostics across different health areas. Whether you’re living with a condition or are a healthy volunteer, your participation could play a vital role in advancing medical research.
About This Trial
This study is designed to evaluate a new approach to treatment, aiming to improve how certain health conditions are diagnosed, managed, or understood. Participants will contribute to important medical research that could benefit future care and innovation.
You don’t need to have a specific condition to take part — some studies are open to healthy volunteers too.
About This Trial
This study is designed to evaluate a new approach to treatment, aiming to improve how certain health conditions are diagnosed, managed, or understood. Participants will contribute to important medical research that could benefit future care and innovation.
You don’t need to have a specific condition to take part — some studies are open to healthy volunteers too.
A clinical trial is a carefully planned research study that tests how well a medical approach—such as a new drug, vaccine, treatment, or medical device—works in people.
These studies follow strict rules to check if the approach is safe, effective, and better than existing options. Clinical trials often take place in hospitals, clinics, or research centres, and participation is always voluntary.
At Clinicalysis, your safety is our highest priority.
We only work with clinical trials that meet strict regulatory and ethical standards. Every trial we support is reviewed by independent ethics committees and regulatory authorities before it begins. We monitor trials closely to ensure they follow Good Clinical Practice (GCP) guidelines, and we keep in regular contact with participants so that any concerns or side effects are addressed quickly. Your health, privacy, and informed consent are at the centre of everything we do.
Eligibility depends on the specific requirements of the clinical trial. Each study has set criteria—called “inclusion” and “exclusion” criteria—that outline who can take part. These may be based on age, medical history, current health status, or other factors. If you’re interested, our team will guide you through a simple screening process to see if you meet the criteria for a suitable trial.
Informed consent is the process of making sure you fully understand a clinical trial before you decide whether to take part. You’ll be given clear information—both in writing and verbally—about the purpose of the study, what will happen during it, any possible risks or side effects, and your rights as a participant.
You’ll have the chance to ask questions and take time to decide. If you choose to join, you’ll sign a consent form to confirm you understand and agree. Taking part is always voluntary, and you can withdraw at any time without affecting your usual medical care.
Yes. Taking part in a clinical trial is always voluntary, and you have the right to withdraw at any time—without giving a reason and without it affecting your regular medical care. If you choose to leave a study, the research team may ask if they can still use any information collected up to that point, but the decision will always be yours. Your safety, comfort, and choice come first.
In most clinical trials, your GP will be informed if you take part—especially if it’s important for your ongoing medical care. This helps ensure your GP has a complete picture of your health and any treatments or medications you may be receiving. You’ll be told exactly what information will be shared and asked for your permission before any contact is made. Your privacy will always be respected.
Some clinical trials offer compensation for your time, travel, or other expenses related to taking part. The amount and type of compensation varies depending on the study and is always explained before you decide to join. You’ll receive clear information about any payments, reimbursements, or benefits in your participant information sheet, so you can make an informed decision.
A placebo is a treatment that looks like the real treatment but doesn’t contain any active medicine. It’s used in some clinical trials to help researchers compare results and see whether the real treatment works better than no treatment at all.
Randomisation means that participants are assigned to different treatment groups by chance, like flipping a coin. This helps ensure the results are fair and not influenced by personal choice or bias. You’ll always be told if a trial involves placebos or randomisation before you decide to take part.
We are always recruiting participants for a variety of studies. Whether you are living with a medical condition or are a healthy volunteer, we may have a study for you.
