Clinical Research & Clinical Trials: Academic Perspective

Clinical trial is a part of clinical research that follows a regulated protocol, or plan of action. Clinical trials are primarily performed to get data on safety and efficacy of the new developed drug, this data is mandatory for further approval of the drug and to bring it into the market.

 

The clinical trials market has been estimated to reach USD 14.2 billion in 2016 and is projected to reach around USD 22 billion by the year 2021, growing at a CAGR (compounded annual growth rate) of 7.5%, during the forecast period 2016 to 2021. Key drivers impacting the market growth are globalization of clinical trials, development of new treatments such as personalized medicine, augmenting evolution in technology, and boosting demand for CROs to conduct clinical trials. Clinical studies can be sponsored, or funded, by pharmaceutical companies, academic medical centers, voluntary groups, and other organizations, in addition to Federal agencies such as the National Institutes of Health, the U.S. Department of Defense, and the U.S. Department of Veterans Affairs. Doctors, other health care providers, and other individuals can also sponsor clinical research.

 

 

  • Trials on Biologics and biosimilars
  • FDA conduct of clinical investigator inspections
  • Meetings with the FDA—Why, When and How
  • Misconducts of clinical trials
  • Perils and Pitfalls of miscommunication in research
  • Community outreach and education in clinical trials
  • Clinical research in academic level
  • Pharma’s role in Bridging clinical research and health care
  • Real world clinical trial strategies and results
  • Informed consent for trials
  • Preclinical research considerations
  • Trends & perspectives in clinical research
  • Brexit’s Impact on clinical research

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