What is Pharmacovigilance writing?
Pharmacovigilance medical writing deals with every aspect of drug development starting from clinical trial through, the essential report submission prior to market authorization and then the post marketing phase. Trained writers are required who apply their functional expertise and clinical drug development knowledge to deal with the technical specifications of the document so that the final proof of the document is legitimate and as per the guidelines issued.
Safety is what an individual seeks. From our day to day living and more importantly in the drugs we consume for our benefits. It would be surprising to know that the drugs/medicines we consume at times can cause adverse reactions in certain individuals. This is where Pharmacovigilance plays a very important role in detecting, analyzing, assessing and preventing adverse drug reactions and in turn improving the patient care and public health by following stringent steps to curb unintended and harmful effects of the drug by dealing with every aspect of the drug lifecycle – from preclinical development to post-market surveillance – making it an essential element in drug research.