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Pharmacovigilance, also known as drug safety, is the science of understanding the adverse effects caused by a drug and assessing whether the benefit will outweigh the peril. This includes detection of adverse effects during the clinical trials and post marketed phases, monitoring and updating the risk-benefit ratio determined upon relevant findings, prevention or minimization of adverse effects, and most crucially, harmonized communication of those findings to the affected global regulatory authorities during a timely manner.

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dakeomkar11

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Types of human resources required in clinical research?

Human resources that are required in clinical research include test subjects willing to undergo the clinical research and doctors, nurses, and technicians who actually apply the techniques.


Why there is lack of clinical research?

There are several reasons for the lack of clinical research, including limited funding, regulatory hurdles, ethical considerations, and a lack of participants willing to enroll in studies. Additionally, research may be focused on more profitable areas, leading to gaps in certain fields. Collaboration between researchers, healthcare providers, and policymakers is essential to address these challenges and promote more robust clinical research.


Is PAREXEL a clinical research company?

Hi,PAREXEL is a Clinical Research Company...BY,Informatics Outsourcing - We are providing spectacular clinical research services such as,Physician Profiling and Web Mining Clinical investigators profiling servicesPrincipal investigators profiling servicesKOL profiling servicesKOL database creationKOL database maintenanceMedical Content WritingBio statisticsClinical data management


What does FDC mean in clinical research?

FDC stands for Fixed Dose Combination in clinical research. It refers to a drug product containing two or more active ingredients combined in a fixed ratio in a single dosage form. This combination therapy can simplify treatment regimens, improve patient adherence, and enhance therapeutic efficacy.


What are Safety and efficacy in clinical research?

Safety of a drug is a measure to check how safe is the drug for human consumption. Safety involves the determination of the toxicity of the drug is and its side effects. Efficacy is the measure to check the effectiveness of the drug to treat the disease at the prescribed doses. Determining the safety and the efficacy of the drug is the one of the main goal of clinical research. Know more about clinical research: http://www.crocareers.in

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A Clinical Research Training Program consists of people performing and learning clinical research. They have to plan their own clinical research and present it. Theses are people learning about how to do clinical things. You must sign up to be involved.


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How do you pronounce the word Pharmacovigilance?

farmakovigelens


What is a brief definition of the word 'pharmacovigilance'?

The definition of the word pharmacovigilance is the assessment of the safety of drugs. This can be in the development pipeline, or in the post-marketing phase.


clinical research?

Clinical research is the study of health and disease in people to help improve health and care


When was Community Programs for Clinical Research on AIDS created?

Community Programs for Clinical Research on AIDS was created in 1989.


When was Mallinckrodt General Clinical Research Center created?

Mallinckrodt General Clinical Research Center was created in 1925.


Types of human resources required in clinical research?

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What document was amended in 2008 pertaining to clinical research ethics?

What document pertaining to clinical research ethics was amended in 2008