Participate In Study
Participate In Study
globeELIXIR suggests and encourage voluntary research studies, conducted in people and are designed to answer specific questions about the safety and for effectiveness of drugs, vaccines, other therapies, or new ways of using existing treatments.
Clinical trial is the scientific term for a test or study of a drug or medical device in people. These tests are done to see if the product is safe and effective for people to use. Doctors and other health professionals run the tests according to strict rules set by the Food and Drug Administration (FDA). FDA sets the rules to make sure that people who agree to be in the studies are treated as safely as possible.
globeELIXIR operate under standard SOPs and management to ensure consistency, safety and quality and follows strict ICH-GCP Guidelines.
Each study has its own rules about who can or who should not participate. This is called “inclusion criteria.” Your eligibility may be based on your age, gender, overall health, type and stage of a disease, treatment history, and other conditions. Not everyone is chosen to participate.
Volunteer
We need healthy or targeted volunteers for paid clinical trials, globeELIXIR is one of the leading Contract Research Organization (CRO), We suggest research programs with the help of paid volunteers as per client requirements to aid the development of new medicines on behalf of the world’s leading pharmaceutical and biotechnology companies.
Volunteers wanted for paid clinical trials We are currently suggest volunteers to take part in our client research studies held at our client centres and get paid to participate in clinical drug trials.
As you are a volunteer, we are suggesting and helping to find a cure or simply improve the standard of living for millions of people and sufferers of varying medical conditions worldwide. On enrolment you will paid for the participation on studies, appropriate medical assistance will be provided during the study. Both male and female volunteers are welcome to participate in the studies and we suggest them accordingly.
If you are participating in a trail, you have to sign an informed consent form. An informed consent for a clinical trial is a more specialised consent and it has a very distinct purpose, it is designed to protect you. You will be given an informed consent document as part of a conversation you have with the research staff before you participate in a trial. The informed consent will explain, all about risks and benefits of the trail and does not obligate you to participate in the clinical trial. Even though you sign the consent, you can change your mind and leave a study at any time.
if you are interested in becoming a clinical trial volunteer, mail us: info@globeelixir.com