Medical software for computers has been a vital tool for many health care professionals for several years now. From EMR software to practice management to specialized diagnostic and surgical programs, physicians, nurses, surgeons, EMTs and other members of the medical industry consider these programs absolutely indispensable. In fact, the government has even decided to mandate that doctors “go digital” over the next few years. One notable holdout has been the FDA, or Food and Drug Administration. Despite the fact that computers are everywhere nowadays, the FDA has continued to allow paper filings from physicians, drug companies and medical device makers who need to report problems with products that have already hit the market. Now, however, the government agency is seeking to incorporate medical software into their standard reporting protocol.
Essentially, the FDA wants to make electronic reporting mandatory in the interest of patients who may be affected by flawed or faulty drugs, devices or products. According to an online posting from the FDA, requiring these reports to be filed online will “help lead to faster identification of potential safety problems.” In addition, it seems that an electronic method would allow health care professionals to communicate their findings and concerns more efficiently, and prevent certain reports from being lost, overlooked or tied up in processing.
It seems clear that the FDA should take the plunge and go electronic. While drug companies and device manufacturers have had the option of filing these reports online since the year 2000, making the use of specialized medical software mandatory seems like a step in the right direction for all parties involved. Government agencies like the FDA should be leading the charge when it comes to digitizing the medical industry, not falling behind the times. Implementing this change would be an excellent way to begin doing just that, and securing the health and wellbeing of millions of patients to boot.