How can clinical trials be more efficient?

February 19 2021

Clinical Research Course is a part of research studies and is conducted on volunteers in order to answer specific questions and get the results of scientific experiments. The trails are non-other than experimenting the newly experimented drugs and testing of its authenticity and safety on human beings. It is one of the medium to identify whether a new drug is safe for the further widely use on a community or group of people. It is also one of the safest and fasted methods of identifying whether the invented drug is working properly and it does not have any side effects on human beings.

Preparing reports on clinical trials are important and should be kept in records for further studies. Overall, it costs millions to billion dollars to the company for conducting the clinical trials and it is not necessary that all clinical trials will give the desired results. It has been observed that 98% of the clinical trials get failed during the initial stages and results in further experiments. However, the successful trials that give satisfactory results prove to be a breakthrough in the healthcare sector. It is therefore important that clinical trials should be conducted in an efficient manner to get the desire results. Moreover, the chances of its success are less due to its prehistoric methods of conducting the research.

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The ways through which clinical trials can be made more efficient through the proper stage-wise process, that is explained below.

Proper designing and registration process- The clinical trial process should be designed in such a manner that all the required information should be made available once the research gets completed. Proper registration process from the regulatory bodies should be made easy to attract more participants involved in the clinical trial. Here, the participants are termed as companies involved in the research and development process.
Participants Enrollment- Participant mentioned are the volunteers, who are ready to get enrolled for the trails. A proper record of the participant's health and their previous medical history should be thoroughly checked and monitored during the trial process. In order to get proper results, a record of ill volunteers and healthy volunteers should be maintained for comparison and stud purpose. A proper record and data will help in identifying the advancement of drug and its therapeutic nature.
Completion of a research study- Upon completion of the study, the records should be made easily available that will help in finding the trials. The trail may be a success or failure will have a proper record of the trial process. In case of death of the volunteers or any change in the medication, the process should be maintained to get a clear picture of the study.
Publication – Publication of data is important and should be made publicly available to understand the progress of the trial. However, due to confidential in nature, these data are publicly unavailable in the open-source. Availing the data will help in avoiding duplicate and repetition of research.
Regulatory- Norms and regulations by the regulatory body should be not made stringent. However, proper monitoring and approvals should be made easy and affordable for the pharmaceutical companies. Introducing such policies will attract more companies in the active participation and direct approach towards research and development process.