Clinical Research

Who’s WHO In Clinical Research?

Who’s WHO In Clinical Research?

Who is WHO?  The World Health Organization is a specialized agency of the United Nations (UN) responsible for international public health. Headquartered in Geneva, Switzerland, the organization’s central focus is to act as the primary governing authority in the international public health domain. As per the WHO Constitution, which establishes…

Importance of Pharmacovigilance during a pandemic

Importance of Pharmacovigilance during a pandemic

Importance of Pharmacovigilance during a pandemic Pharmacovigilance can be simply defined as the intense supervision and monitoring of a drug or drug related products during its clinical trials and thereafter its launch to the market. Pharma comes from a Greek word Pharmakeia which means drugs, medicines, or remedies and vigilance…

The Evolution of Clinical Data Management

The Evolution of Clinical Data Management

The quality of clinical trial data and clinical trials has been deteriorating continuously over the years. To preserve this proficiently, several CDM organizations have evolved to improve data leadership working within a digital environment with more tactical and prolonged functions. During the process of coding and reconciliation, patient data collection…

Roles and responsibilities of a clinical research coordinator

Roles and responsibilities of a clinical research coordinator

Who is a CRC? A Clinical Research Coordinator (CRC) is a person responsible for conducting clinical trials using good clinical practice (GCP) under the instructions from a Principal Investigator (PI). A health care professional who, under the supervision of the investigator, submits all research documents to IRB, schedules and implements the study visit requirement, co-ordinates all…

E-learning: Pharmacovigilance In India

E-learning: Pharmacovigilance In India

Pharmacovigilance is a science of detecting and reporting adverse drug reactions, adverse events, and abnormal laboratory findings. Prior to release into the market, all new medicines/ medical devices must have completed a series of clinical trials with patients. These trials are aimed to establish the safety and efficacy of the…

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