This is a general category for clinical research
What are Clinical Trials :- Clinical trials experiment includes sequence of tests integrated in therapeutic research and new drug development that helps produce safety and efficacy information (or more purposely, data pertaining to adverse drug reactions and adverse effects of novel interventions) for treatment measures (e.g., therapeutic drugs, medical diagnostics, health care devices, therapy protocols).
What are the key tasks of a Clinical Research Associate in Clinical Trial experiments? CRA Training :- A CRA (Clinical Research Associate) is responsible in design, scheduling, preparation, execution and review of a clinical trial experiment to guarantee it that it sticks to regulatory and ethical guidelines. CRA’s also play a key role in data exchange with all the stake holders.
Good Clinical Practice (GCP) Training is mandatory for all people actively working in the clinical research industry. Enrolling in a online GCP course is a good idea if you intend to work or are already working on clinical trials. You may be working at a site level as a clinical study coordinator, pharmacist, principal investigator, Co-investigator etc, or you may […]
Clinical research education in USA, UK, Canada and other developed countries is offered by many clinical research training providers. The nature of these training providers ranges from autonomous institutes to universities to contract research organizations and it is often difficult to decide which program to enroll in. Which program suits you best depends on your own preferences and criteria. If you are […]
Clinical trial outsourcing is a boon to the western drug companies since developing countries not only ensure cheaper trial costs but also offer crucial savings on time to market. Conduct of clinical trials in developing nations does require some improvement in terms of regulatory aspects but they undeniably offer a lot of advantages, which have attracted the pharmaceutical industry from […]