Clinical Research

Clinical trials are medical research studies involving people. They aim to test whether different treatments are safe and how well they work. Some trials involve healthy members of the public. Others involve patients who may be offered the option of taking part in a trial during their care and treatment. Clinical trials are carried out to try to answer specific questions about health and illness. Clinical trial is a systematic investigation in human subjects for evaluating the safety & efficacy of any new drug. Clinical trials are a set of tests in medical research and drug development that generate safety and efficacy data for health interventions in human beings.  

Four phases of clinical trials and medicine development exist and are defined below.

Phase1: It is the first stage and usually involves small groups of healthy people or sometimes patients. Phase 1 trials are mainly aimed at finding out how safe a drug

Phase2: Objectives focus on dose-response, type of patient, frequency of dosing, or numerous other characteristics of safety and efficacy.

Phase3: clinical trials generate data on both safety and efficacy in relatively large numbers of patients in both controlled and uncontrolled trials.

Phase4:  Trials conducted after a medicine is marketed to provide additional details about the medicine's efficacy or safety profile. Different formulations, dosages, durations of treatment, medicine interactions, and other medicine comparisons may be evaluated.

  • Preclinical trails
  • Phases of clinical trails
  • Optimum dose finding
  • Single ascending dose limits
  • Multiple ascending dose limits

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21st Annual European Pharma Congress

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Clinical Research Conference Speakers

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