Topic > How could we work on an industrial level while minimizing risks for patients in legal standards

We could produce cyber healthcare in OECD orthopedics clinics every year to describe the parallel functioning of similar informal channels in the network of OECD, i.e. with many similar standard processes repeated in similar preoperative, operative and postoperative healthcare. It could be achieved in gradual proportional sampling - when we could define stratified clusters of similar Orthopedic Clinics with subsequent internal sampling - for example of 3% in proportional sampling - Patients of the sum of the number of orthopedic patients hospitalized in the year XXXX, which were at least 3 days of healthcare in a hospital bed - with standard types of orthopedic operations performed - for example total hip arthroplasty, total knee arthroplasty, replacement of skeletal spinal elements, repairs of hip arthroplasty, knee arthroplasty, etc. Say no to plagiarism. Get a tailor-made essay on "Why Violent Video Games Shouldn't Be Banned"? Get an original essay In OECD orthopedics clinics we could recognize similar main streams of main repeated standard medical classes of medical tasks of orthopedists, radiologists, managers, capabilities who collaborated Planners, capabilities of intensive unit departments Healthcare, medical activities and medical personnel in operating rooms, etc. - through the use of similar diagnostics and similar recommended treatments, similar Medications, efficient and modern mass implementation of Medical Devices, technical and IT equipment in the workplace with usage practices compliant only with the technical requirements of the law, on exact invoices of the manufacturer, with user company installing instruments, firm x-ray masks, measurements of the right positions of orthopedic devices implants in the bones - from the same clinical processing - as they were used in the medical processing tested in the clinical tests of each new medical device with final approval of FDA rules or according to "CE" rules_marking through conformity assessment in EU states. You ignore the sharing of elementary and profound medical results and competent in the medical processing of the development and clinical testing stages of medical devices so as to forget, in the next user practices, even worse the fuzzy sharing of the origin information from the models of approval? WHY? We have user-educated medical and nursing staff, such as certified health care providers with medical staff - but with repeated and massive similar medical errors in decision making - in OECD orthopedics clinics, we could define the typical annual statistical structure of orthopedic diseases. Incoming orthopedic patients in the comparison years 2016, 2018. 2020 - mostly with similar locomotion and complicated additional neurological problems - in similar fixed cases of Cluster Orthopedic Patients, i.e. for typical important differences in age, gender, private personal weight , skeletal structure with similar deformities, with typical coincidences with other further parallel problems for medical decision making: i.e. with frequent patients with high blood pressure, with frequent diabetes melitus, with often repeated bone osteoporosis_of patients older than 65 years, with circulation critical blood vessel with thrombotic blood vessels similar multilateral risks, with heart weakness often personal, cardiac arrhythmia, health problems state after some light strokes, sometimes with presence of horrible diagnoses HIV, TB, hemorrhagic infections, typical polytraumatic health problems after traffic accidents , motor injuries !