The establishment of CRO in India is a very important step in the discovery and development of new drugs in the medicine department. The CRO Company or the Contract Research Organizations are a type of company that helps in undertaking the entire responsibility of the clinical trials. The clinical trial is a process that is conducted on the invention of a new medicine, drug, or a vaccine. For example, a scientist discovers a new drug that shows the positive results for treating the symptoms of particular disease. Then it would be sent to the department of CRO for clinical testing and pre-clinical treatment for ensuring the safety of the drug on the patients.
Thus, this article would further emphasize on functions of the CRO company and the independent auditors for CRO.
- Finding the sponsors for the clinical trials procedure
The procedure of clinical trials might involve a lot of money in the different steps and stages. There are many types of machines and tools required for this procedure to be executed. Thus, the CRO company would help in finding suitable sponsors for the efficient treatment. This would help the treatment to be executed without any kind of financial concerns.
- Ensuring complete safety of the patients
The establishment of CRO in India also ensure the safety of the patients on whom the clinical trial would be conducted. The safety is the topmost priority of the CRO Company. Thus, it would help in analyzing any kind od possible threats or risks on the patient prior to the clinical trial.
- Monitor patient data after the procedure for avoiding any side-effects
The CRO would also monitor that patient’s data with the help of independent auditors for CRO after the trial has been conducted. The patient’s body might react to the treatment so that is required to be monitored.
- The adaptivity of the new information to streamline it into the new drug formation
As soon as the pre-clinical treatment is done, the CRO Company takes up the responsibility of using the giving information into the formation of the new drug. Thus, the procedure of a new drug starts with the acquired information.
- Approval of the clinical drug by FDA and other departments
The clinical trials are executed in a successful manner only after the proper regulatory formalities are done. The approval from the FDA and other departments is achieved with the help of the CRO Company.
- Send the new drug to the market but keep it in track to notice any bad results on patients
Once all the other formalities are completed and the clinical trials is well-executed, the new drug is given an existence. The next duty of the CRO Company is to supply it into the market. This is done in a manner that it is even distributed in different parts. The work of CRO is not over till yet. They also keep a keen check on any kind of reactions and results on the consumers of the newly formed medicine.