EmcrownAbout Clinical Research
Unlocking Tomorrow’s Breakthroughs: What Does Clinical Research Entail?
About Clinical Research
- What is it?
Clinical research is the meticulously supervised process of assessing the safety and effectiveness of promising new medications and therapies for preventing, treating, and managing diseases that affect humanity. It employs all ethical and legal requirements to protect participants.
- How does it work?
- Interested participants will be given details of the study to review and ask questions before deciding whether to continue. (You can always ask your study doctor questions throughout the study).
- Participants will sign an informed consent to indicate an interest to continue. (Consent can be withdrawn at any stage of the study process by informing your study doctor).
- Participants will be screened to determine if the study is suitable for them.
- During the treatment period, participants will visit the clinic, where they will be closely monitored and assessed throughout the study's duration. Participant safety is paramount!
- After the study ends, participants will receive follow-up care and safety monitoring.
- Why participate?
- Become a pioneer! Be first to timely experience potentially new cures to diseases that are not yet available to the public.
- Free access to treatments! Receive some stipends and study-related care from medical experts at no cost.
- Monitor your health! The trial process involves frequent check-ups that help keep track of your health.
- Stipends! Get some compensation for your time and participation.
- Volunteer for a worthy cause! Every current medical breakthrough was enabled by clinical trials. Participating makes you a catalyst for breakthroughs.

- Patient Safety
Every trial is highly regulated with mandatory and strict ethical and legal standards. The FDA is the primary regulator, and Independent Review Boards review and scrutinise all aspects of a trial as required by law.
Learn more about our patient safety management.