Omnicell

JANUARY 10, 2023

Standardizing an interoperability solution that supports information exchange creates better medication management practices for nurses and improved patient engagement. Before the integration, medication dispensing typically occurred without a conversation at the patient's bedside. Subscribe today.

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Omnicell Cerner Medication Dispensing Documentation 98

Omnicell

JANUARY 10, 2023

The Chief of Anesthesia is now aware of flaws in documentation and has an awareness of open transactions through enhanced data visibility. The Omnicell Blog is the leading source for pharmacy care, exploring emerging trends, successful best practices, and ideas and insights focused on the digital transformation of pharmacy.

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Omnicell Medication Dispensing CPhT Documentation 52

Omnicell

JANUARY 10, 2023

Local pharmacists have always strived to be more than medication dispensers. Crucially, CareScheduler keeps patients and staff safe during the pandemic by minimizing the physical time spent in the pharmacy filling out and signing paper documents. Click here to learn more about EnlivenHealth.

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Community Pharmacies Patient Care Medication Dispensing Vaccines 52

Omnicell

JANUARY 10, 2023

In a manual environment, you'll also see redundant documentation when an anesthesia professional is required to document all the administered medications on paper, then again in the electronic health record. A more reliable, technology-driven approach can support better outcomes and safety in the operating room.

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Controlled Substances Omnicell Medication Dispensing Documentation 52

Omnicell

JANUARY 10, 2023

Omnicell has continued to refine medication workflow with the XT Anesthesia Workstation™ , and new functionality helps both parties accomplish this goal. We’ve developed closed-loop functionality that makes it easier for providers to document waste, improving the likelihood of compliance.

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Controlled Substances Omnicell Medication Dispensing Documentation 52

The FDA Law Blog

OCTOBER 17, 2023

Background The Breakthrough Devices Program, established under section 515B of the Federal Food, Drug, and Cosmetic Act (FD&C Act), is a voluntary program for certain medical devices and device-led combination products. By Philip Won & Lisa M. Wysa, see here ) and addiction (e.g., reSET-O, see here , here ).

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Documentation FDA Medication Dispensing Hospitals 53

The FDA Law Blog

SEPTEMBER 26, 2022

FDA published a proposed list on June 13, 2018 (83 FR 27609), which we blogged about here. much like an FDA guidance document. Some low-risk devices are exempt from cGMPs except for complaint handling and record keeping requirements, e.g. , a liquid medication dispenser ( 21 C.F.R. 880.6430 ).

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FDA Medication Dispensing Documentation Packaging 40