Eice(BYOD). There are advantage and disadvantages for provisioned and BYOD mobility. What is the future? Its predicted that technology will exist within the next 5 years that projects the full vital signs of patients. From a regulatory point of view the safety of the patient is priority. The concern would be that if we can measure this confidential data, then how long will it be till it becomes mandatory to collect such data? This will allow a real time record of data which was unavailable previously in the past. Medical motors may make final decisions for the patient based on this data….
Read More >
Two of our consultants recently represented KVALITO at the 15th DIA Conference on European Electronic Document Management, held on December 2-3 in Berlin, Germany. A wide range of interested parties attended the conference, from big pharma (Pfizer, Sanofi, Bristol-Meyers Squibb, GSK, Bayer, Novartis, Roche), health authorities (FDA, BfArM, Egyptian Ministry of Health, MHRA), providers and vendors, to hear new information about electronic document management in the area of clinical trials and pharmacovigilance. Key topics that emerged from the conference presentations and discussions included: Upcoming EU Clinical Trial Regulation: Discussion and presentation about the upcoming clinical trial regulation and its impact…
Read More >