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Contract Clinical Trials

Clinical Research is a medical research involving people. There are two types of clinical research - observational studies and clinical trials.

So, what is a clinical trial? It's a research study conducted in human beings with the objective of answering particular questions about novel therapies, diagnostic procedures or vaccines, or innovative ways of using well-known treatments. The clinical trials are used to conclude whether new treatments, diagnostics, or treatments are both effective and safe.

A good test, like a good clinical trial, frequently has blind controls or double-blind randomization to evaluate the final results. The aim for a well-controlled experiment is for it to be repeated several times with the same or statistically alike results.

All medical trials or clinical trials have risks. But, any medical examination, or process has risks. The risk may be higher in a clinical trial as there are more unknowns. This is mainly true of phase I and II clinical trials, where the treatment has been studied in fewer people.

One of the various main documents that administer the conduct of clinical trials are Clinical trial agreement/Contract clinical trials. They serve as a legally binding contract between a sponsor, site, and researcher, and outline every party's responsibilities and duties for the clinical trial.



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