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.
At Clinicalysis, we know that joining a clinical study can feel overwhelming. That’s why our dedicated team supports you from first enquiry through to your last visit—and beyond. You’ll receive personal attention, flexible scheduling, multilingual support (if needed), and a thorough explanation of what to expect.
You’ll also receive regular health monitoring, and in many cases, access to innovative medical treatments not yet available in standard care. We’ll also stay in contact with your GP to ensure continuity of care.
Identify potential participants through referrals, database searches, advertising, or chart reviews.
Make initial contact (phone, email, in person) to briefly discuss the study, check basic eligibility, and gauge interest.
Provide the Participant Information Sheet (PIS) and explain the trial’s purpose, procedures, risks, benefits, and participant rights.
Allow the patient time to review and ask questions before proceeding.
Conduct the informed consent discussion in detail, ensuring understanding of all aspects of the study.
Answer all questions, confirm voluntary participation, and obtain signed consent before any study-specific procedures.
Conduct detailed screening assessments per protocol (medical history, physical exam, labs, imaging, questionnaires, etc.).
Confirm that the patient meets all inclusion criteria and none of the exclusion criteria.
Document screening results and eligibility status in source documents and case report forms (CRFs).
Verify that all essential regulatory documents (signed consent, approvals, training logs) are complete before enrollment.
Perform all required baseline tests and measurements as per protocol (e.g., vitals, bloodwork, imaging, disease scoring).
Ensure data is complete before moving forward.
Confirm eligibility and baseline data with the Principal Investigator (PI).
Officially enroll the patient into the trial database as an eligible participant.
Use the trial’s randomization system (IVRS/IWRS or other method) to assign the participant to a treatment arm.
Document randomization number, date, and assigned treatment in both source documents and trial database.
At Clinicalysis, volunteers play a vital role in advancing medical research and shaping the future of healthcare. By participating in one of our clinical studies, you’ll be contributing to important scientific discoveries while accessing new treatment options and expert medical care. Every study we conduct is managed with the highest standards of safety, ethics, and confidentiality. If you’re interested in making a difference and being part of groundbreaking research, we invite you to explore our available studies and find out how you can get involved.
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.
