Prepare Yourself For Success By Earning A Postgraduate Diploma

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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 emerging field of pharmacovigilance was out of reach in regions of the world such as Brazil, Russia, China, India, the Middle East and Singapore. But today institutions such as the James Lind Institute are making advanced PG diplomas and training in these fields available to students in these parts of the world.
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Clinical research associate training Online

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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 in life science, pharmacy or medical sciences. In infrequent cases, corporate will pick personnel with nursing degree with a registered certification. Continue reading

Clinical Research Associate Education

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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 science, or health discipline. In rare cases, companies may choose candidates with nursing qualification with a registered nurse certification. Continue reading

A Relentless Field of Pharmacovigilance in India- Now a Demand!

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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. Continue reading

Clinical Research edges to attract the people of Brunei

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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. Continue reading

Clinical Research & Regulatory Affairs Courses

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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. Continue reading

Online Training Program in Clinical Data Management (CDM)

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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. Continue reading

What are Clinical Trials

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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). Continue reading

Clinical Research Associate Training (CRA Training)

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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. Continue reading