This is a category for pharmacovigilance courses
Pharmacovigilance is the branch of science that deals with the safety of drugs after they have been approved for use. It basically involves identification, evaluation, monitoring and prevention of adverse reactions associated with the usage of drugs. Pharmacovigilance is an important part of clinical research and plays a crucial role in avoiding drug related disasters and toxicity.
Herbal medicine has been known to be effective in the treatment of various ailments since the beginning of human civilization. Ayurveda is a form of herbal therapy originated in India. Plants, their parts, metabolites and preparations are proven to have enormous therapeutic properties. The importance of herbal medicines has been overlooked with the rise of modern medicine, yet they never […]
The process of collecting safety profile of drugs during or after clinical trials is never complete but is a continuous endeavor. Generally thousands of patients are subjected to clinical trials however in some cases for example if drug gets orphan status few hundred are subjected to drug. In statistical viewpoint, if 1,000 clinical trial
Over view of Pharmacovigilance Pharmacovigilance (PV or PhV) is the science related to the detection, evaluation and prevention of adverse effects of drugs, biologics or medical devices. It includes the study of both short-term as well as long-term adverse effects experienced with the use of a therapeutic in a post-marketing or clinical trial setting. Pharmacovigilance is evolving as a strategic
Study of drug safety and the serious adverse events (SAEs) of drugs is commonly known as pharmacovigilance and off-late it has become a very interesting topic within the pharmaceutical industry. In the newly published FDA document explaining strategic goals for 2011-2015, FDA Commissioner explained:
Pharmacovigilance and Regulatory Affairs are an essential part of the larger health care industry. This article is all about an overview of Pharmacovigilance and Regulatory Affairs departments and what functions both these departments perform.
“A career in Drug Safety /Pharmacovigilance is interesting with a nicely described career path”. The career growth is rapid in this field which gradually brings one to managerial positions with excellent salary packages. Following is defined as what is Pharmacovigilance, what you expected to do as a pharmacovigilance professional, job description (JD), a list of potential employers, wage prospects and […]
Pharmacovigilance Overview Drugs have been formulated and used for hundreds of years but it was only in the 1960’s that it was regarded as essential to carefully monitor the safety of drugs after being marketed. The wake-up call to this realization was the thalidomide tragedy.
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.
Saudi Arabia and the whole of the middle east especially UAE are aggressively positioning themselves in the global contract research arena and have been successful in gaining significant attention of pharmaceutical and contract research companies from the west. Saudi Food and Drug Authority (SFDA) has already issued regulations and guidelines for conducting clinical trials in Saudi Arabia and also issued Pharmacovigilance guideline […]