Whenever there is a new drug that is introduced in the market or a new medical device is launched, have you ever wondered what goes on in the background? What happens before FDA approved to be sold in the market? Well! The answer is, before a drug or a device is sold in the open market is declared safe, a huge amount of planning, research and data goes in clinical trial before the drug is safe to be sold. As a layman, you must be thinking that some hospital or pharmaceutical company is behind the invention. It is not completely wrong. Pharmaceutical companies sponsor clinical trials to create the drug and bring it into the market.
Clinical trial is a process in which set of medical professionals, biotechnical engineers and other related parties brainstorm together to formulate a new medicine or device that could cure the patient quickly and at minimum costs. There are different phases of a trial and at every phase is requires Clinical Trials Monitoring by research auditors designated by CRO.
Clinical Trial Monitoring is a challenging job because the decision made during the trial would impact lives of many human beings. Hence, these people need to be highly skilled, educated and experienced to monitor trials. These auditors even act as mediator between the researchers and the sponsor. They are expected to closely monitor each and every phase so that there are no surprises during the trial.
Being a Clinical trial associate requires Training In Clinical Trials from institutes specialising in this form of study. Since India is becoming the focal point for research and development in medicine, there are many institutes today where you can formally get trained to be a clinical research associate.
But even before you choose this profession; keep in mind that being a CRA is not easy. It is requires great deal of dedication, hard work and commitment. Therefore, take your decisions wisely.
For More Information Visit Here: http://www.crimson.org.in/monitoring-clinical-trials.html