Output Of The Post Market Surveillance (PMS) Plan
The Need for PMS Post Marketing Surveillance (PMS) are often defined because the process of identifying and gathering information concerning medications or medical devices after it's been approved by the concerned authorities like the Food and Drug Administration (FDA) within the US. With regards to medications, a scientific PMS process commenced way back within the early 1970s and since then, there has been a considerable increase in PMS. Drug and medical device monitoring following the method of approval has become mandatory for several reasons (FDA, 2020). Way back within the past during the 1950s and 60s, the amount of medicine within the market were very scant compared to today which made monitoring a rather easy process. within the present day, drug manufacturing has assumed magnanimous proportions and is being consumed at a really high rate. Several other factors that warrant the necessity for PMS pertains to the modifications within the approval process of the FDA.