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EMMA CLINICAL RISK LOG Risk No. Date raisedRaised by101/04/15EPMA teammate transfer of patients between wards using EMMA and wards that are not using Tamarisk of delayed/missed doses due to confusion
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How to fill out epma clinical risk log

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How to fill out epma clinical risk log

01
Open the EPMA clinical risk log template.
02
Enter the date and time of the risk assessment.
03
Identify the patient's name and unique identifier.
04
Write down the clinical risk factors associated with the patient.
05
Assess the severity of each risk factor on a scale of 1 to 5.
06
Evaluate the likelihood of each risk factor occurring on a scale of 1 to 5.
07
Calculate the risk score by multiplying the severity and likelihood scores for each risk factor.
08
Summarize the overall risk score for the patient.
09
Provide any additional comments or observations regarding the patient's clinical risk.
10
Obtain necessary approvals and signatures.
11
Save and submit the completed EPMA clinical risk log.

Who needs epma clinical risk log?

01
Healthcare professionals involved in patient care and treatment.
02
Clinical risk managers and quality improvement teams.
03
Hospital administrators and compliance officers.
04
Medical researchers and academic institutions.
05
Regulatory bodies and government agencies overseeing healthcare quality and safety.
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Epma clinical risk log is a document used to record and monitor clinical risks associated with the use of Electronic Prescribing and Medicines Administration systems.
Healthcare professionals and organizations using Electronic Prescribing and Medicines Administration systems are required to file the epma clinical risk log.
The epma clinical risk log should be filled out by documenting any potential clinical risks, their impact, and any mitigating actions taken.
The purpose of the epma clinical risk log is to proactively identify and manage potential clinical risks associated with Electronic Prescribing and Medicines Administration systems.
Information that must be reported on the epma clinical risk log includes clinical risks identified, their potential impact on patient care, and any actions taken to address them.
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