Electronics Healthcare Provider Patients Safety 
PM360
SEPTEMBER 7, 2023
1 For 65% of respondents, one of the biggest issues was that coordinating and managing healthcare is overwhelming and time-consuming. A similar number of respondents (64%) expressed disappointment with their interaction with physicians, wishing that healthcare providers took more time to understand them.
Referral MD
FEBRUARY 15, 2024
. “The sharing and administrative functions of coordinating healthcare lag decades behind. 75% of patient information in the US is still exchanged via fax, costing US healthcare billions of dollars yearly…and more importantly, compromising patient safety and provider job satisfaction.”
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Impetus Digital
JULY 5, 2023
Cloud technology in healthcare has become critical in improving patient care and revolutionizing healthcare systems. Patients are more willing than ever to seek out greater healthcare services if their expectations are not met. Thus, the healthcare industry is taking a more proactive approach.
Pharma Marketing Network
MAY 15, 2023
With the advent of electronic health records, social media, and other digital sources, pharmaceutical companies now have access to vast amounts of data that can be used to inform their marketing strategies. One of the biggest challenges is ensuring that patient privacy is protected.
Pharma Marketing Network
MARCH 23, 2023
With the advent of electronic health records, social media, and other digital sources, pharmaceutical companies now have access to vast amounts of data that can be used to inform their marketing strategies. One of the biggest challenges is ensuring that patient privacy is protected.
Nixon Gwilt Law
APRIL 22, 2024
The rule applies to developers of Certified Electronic Health Record Technology (CEHRT), particularly those who incorporate predictive decision support interventions (DSIs) into their products. Valid: Confirms that DSIs are scientifically and statistically sound, providing reliable predictions based on the data and methodologies employed.
European Pharmaceutical Review
SEPTEMBER 2, 2022
To ensure the safety of medicines post-regulatory approval, a risk management plan (RMP) is established. An RMP is submitted as part of the dossier of all new drug applications and is evaluated by regulatory authorities before authorisation is given. What are risk minimisation methods?
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