pharmacovigilance

The FDA describes the term pharmacovigilance to mean "all scientific and data gathering activities relating to the detection, assessment, and understanding of adverse events."

Big Pharma Hits On Pregnant Women 2006

Tshabalala-Msimang said various sections had also been added to the book, and included "pharmacovigilance" - the detection and reporting of adverse drug reactions.

ANC Daily News Briefing 2004

This means, in fact, that the pharmacovigilance, that is the supervision of the medicinal results in their usual conditions of use, has not been favourable to it.

Chapter 12 1991

The health ministry under the government of India was considering the proposal to set up drug side-effects monitoring centres - or so-called pharmacovigilance centres - in all medical colleges across the country.

DWS Pill Scribe 2010

Instead of using the CSW as an opportunity to find solutions to these problems, Minister Tshabalala-Msimang has instead used every opportunity she has had to resurrect her now thoroughly discredited positions on treatment toxicity, "pharmacovigilance" and "alternative remedies".

open Democracy News Analysis - Comments 2009

Instead of using the CSW as an opportunity to find solutions to these problems, Minister Tshabalala-Msimang has instead used every opportunity she has had to resurrect her now thoroughly discredited positions on treatment toxicity, "pharmacovigilance" and "alternative remedies".

open Democracy News Analysis - Comments 2009

They have looked to us for full service, multi-national program project services in phases III, IIIb and IV, for selective functional services such as pharmacovigilance and pharmacoepidemiology, or for volume-based services through functional service provider contracts over multiple years in the areas of biometrics, state D [ph] medical writings.

Biotech Sector and Stocks Analysis from Seeking Alpha 2008

Linda McAvan MEPLabour European spokesperson on health and rapporteur on pharmacovigilance

Letters: EU drug trials law 2011

It will post new ones quarterly, for a total of about 100 a year, said Robert M. Boucher, a physician in the agency's pharmacovigilance division.

FDA begins to post online the results of evaluations of recently approved drugs 2010

But in addition this view sees article 102 of the Code, which requires national regulators to maintain a pharmacovigilance system to ensure good regulatory decisions having regard to adverse reactions under normal conditions of use, as colouring what information a qualified person must provide.

Archive 2008-03-01 2008