A common question that often comes to mind is whether clinical trials are required to be conducted locally as a stated or implicit condition to obtain marketing approval.
Even before a drug could be tested in a clinical trial, the development process of a drug generally involves three major steps, including discovery, preclinical development, and then clinical trial. The transition from discovery to preclinical development is an ongoing process. The results obtained from toxicology and preliminary pharmacology testing often contribute to candidate selection for a drug. The filing of an Investigational New Drug (IND) sets up a boundary between preclinical development and Clinical Research Courses of a drug.
The following international organizations ensure drug safety and efficacy:
Take Clinical Research Training
Some of the national regulatory bodies issuing guidelines for drug development include:
Principles regulating clinical trials worldwide
Clinical research training programs are designed for clinicians and scientists around the world. These research training programs provide advanced training in healthcare methods and research.
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