Our Blog
We provide complete Analysis on Education for different carrers.
What is Clinical Research?
With the rise in India's healthcare sector, clinical research, a branch of medical science and one of the most knowledge-intensive industries, is developing as a promising career. The Indian pharmaceutical industry is rapidly expanding, and it has become a popular location for international pharmaceutical corporations to perform medication research and development.
Clinical research is an important aspect of the drug discovery process since it ensures that a new medicine is safe and effective. It's the entire story of a medicine, from its conception in a laboratory through its introduction to the consumer market and beyond. Clinical research is the methodical and scientific investigation of the effects, dangers, efficacy, and benefit of a new medicinal product (drug) for the prevention, treatment, diagnosis, or relief of disease symptoms. Clinical research is the process of determining the safety and efficacy of drugs, equipment, diagnostic products, and treatment regimens designed for human use.
Signing and implementation of General Agreement on Tariffs and Trade (GATT) has opened up additional opportunities and has opened market for clinical trials industry. Furthermore, the country possesses a plethora of government-funded medical and pharmaceutical institutions with cutting-edge facilities that could serve as ideal sites for multi-center clinical studies with a large population and large variety of diseases.
Prior to launching in the market pharmaceutical product's clinical study is conducted. Clinical trials are used to test the safety, efficacy, and effectiveness of new biological or behavioural therapies. Each component of the drug approval procedure is handled as a separate clinical study in these trials, which are undertaken in four stages. In most cases, the drug development process will take many years to complete all four phases. If the medicine passes Phases I, II, and III with flying colors, it will be approved by the FDA (Food and Drug Administration) and marketed to the general public. Phase IV studies are referred to as "post-approval" investigations.