The Food and Drug Administration

Crisis Development
January 14, 2023
Recommending an Evidence-Based Practice Change
January 14, 2023

The Food and Drug Administration

Description

I need the following two questions answered

student response 1

BARBARA P.

With the ever-growing advancements in technology and as customer demand and needs change, I only see electronic health record software getting better. The software will become more proficient, efficient, reliable, better user friendly, fewer errors, or even error-free. The price for development and implementation could also become cheaper as efficiencies are improved. With the advancements in medical technology, we may move to an age where there will be no need for electronic health records due to patients being able to store their own electronic health records on chips that can be worn on the body. Physicians, hospitals, and pharmacies would simply have to scan the chip to have instant access to a patient’s electronic health record.

The Food and Drug Administration approved the first implantable microchip almost 15 years ago, however, it is not yet widely adopted. These microchips can store a patient’s entire medical health record (Hughes, 2018). These microchips are beneficial for patients who may present to the emergency room unresponsive. Medical staff can quickly access their medical records including demographics, and critical medical history to properly treat the patient.

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STUDENT RESPONSE 2

REA B.

What is the difference between an RFP and an RFQ? How can they assist in the selection process of a new system?