This is a category for clinical research institutes
Getting the on job training you need to succeed in your chosen career or profession can at times seem difficult if not impossible. Without the help of the Internet, finding a place to start would seem out of the realms of possibility for today’s student. In the past, training for careers in clinical research, medical writing, healthcare and the newly […]
Clinical research is a scientific intensive effort. A clinical research associate (CRA) is a clinical research personnel depicted by ICH GCP (Good clinical practice guidelines). ICH GCP uses the word Monitor in the place of CRA, the two terms are considered to be identical. The requirement for a Clinical research associate career is to have an UG or PG degree […]
Clinical Research Associate Education :-A clinical research associate (CRA) is a clinical trial personnel described by ICH GCP (Good clinical practice guidelines). As ICH GCP uses the term Monitor in the place of CRA, the two terms are well thought-out to be equal. The pre-requisite for a CRA job is to have an UG or PG qualification in pharma, life […]
Clinical study, and Clinical trial both signify the same — a scientific endeavor to find out how a novel drug or treatment works in humans. Through clinical studies, medical practitioners find a novel and a better way to thwart, perceive, identify, manage, and treat ailments.
Pharmacovigilance has had its focus on the many adverse drug reactions known as ADR’s that refers to a sudden, un-predicted response of a drug that can be peril to public health. In due course of time, India lacked the necessary resources to help tackle situations across the country in response to any drug reaction/ side effects.
The purpose of research is the enthusiasm to question an urgent issue or a situation & find answers to the question. The other facet of research is to publicise the work of a committee so that others will learn from what had been done to realize the specified results.
Clinical Research & Regulatory Affairs Courses: As a professional in clinical research and regulatory affairs, you work in a drug discovery company or a public health care units, bearing tasks for documenting and endorsing the worth, effectiveness and safety of new drugs in approval submissions for regulatory. You estimate and document the fulfillment of clinical studies to regulatory requirements.
Online Clinical data management Training -: Clinical data management (CDM) training is generally available as part of a certificate or professional or post graduate diploma programs in clinical research or health care management. On-line or hybrid courses may be readily available as well as in-campus courses.
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.