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Connecting with Patients at Home

Pharmacy Is Right For Me

In addition to learning more about unique pathways on-site, you can also understand more about the career paths of these pharmacists here on our blog. Another unique aspect of this model is that all interprofessional team members can access and document within a universal electronic medical record (EPIC).

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How Advances in Cloud Computing Can Impact Big Data for Pharmacy

Omnicell

For example, in the acute care setting, most medication identification is driven by coding that originated in the electronic medical record (EMR), which is unique to a particular instance of that EMR. That said, normalization of that data is imperative, as inconsistency can lead to semantic dissonance.

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Patient Recruitment – Key Determinant of Successful Clinical Trials

Roots Analysis

However, there are certain emerging techniques, including electronic medical records, mobile applications, patient advocacy groups and social media that are revolutionizing the patient recruitment domain and are expected to reduce the timelines as well as cost of the clinical trials significantly.

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Lots of FDA Guidance, But Few Drug Manufacturing “Remote Interactive Evaluations” (We Would Call Them “Virtual Inspections”)

The FDA Law Blog

Admittedly, BiMo inspections (into items like adequacy of bioequivalence data, consistency of clinical trial data with medical records, and compliance with clinical trial protocols) lend themselves better to an RIE than assessing manufacturing compliance with regulatory requirements.

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How Digital Transformation Is Affecting The Pharma And Healthcare Industry?

Fossil Remedies

Read the blog further. They can have online access to their medical records as well. These advancements will start a new era that will lead to a new phase in the history of healthcare. Want to know about some points that underline the digital transformation? Changing the role of patients in the treatment.

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When Worlds Collide: The Theory of Real-World Evidence Meets Reality

The FDA Law Blog

There is ample data collected on them during this 24/7 monitoring period such as case notes, contemporaneous patient medical records, and patient tapes. Every use of ESD is recorded, as is every behavior that falls within the intended use. Patients that use ESD undergo continuous 24/7 monitoring.

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When Should a 510(k) Include Clinical Data?

The FDA Law Blog

electronic health records, claims). These include: results of pre- and post-market clinical investigation(s) of the device (i.e.,

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