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Medical Device Alert MDA/2019/017Issued: 20 March 2019 at 11:00Pagewriter Cardiographs (TC20/30/50/70) manufactured before 20 November 2018 and Official Monitors (CM10/12/100/120/150) manufactured
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Anyone in the pharmaceutical industry or healthcare sector who wants to stay informed about MHRA alerts can benefit from epharmalert.
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This includes but is not limited to pharmaceutical companies, healthcare professionals, pharmacists, regulatory bodies, and medical device manufacturers.
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MHRA alerts contain important information about potential risks, recalls, or safety updates related to medicines or medical devices, making them crucial for ensuring patient safety and regulatory compliance.
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By using epharmalert, these stakeholders can receive timely notifications and access relevant alerts to take appropriate actions and stay up-to-date with the latest regulatory information.
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MHRA alerts - ePharmAlert is a notification system used by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK to inform healthcare professionals about important safety information, recalls, and risk assessments regarding medications.
Healthcare professionals, pharmaceutical companies, and any stakeholders involved in the distribution and administration of medicinal products are required to file MHRA alerts - ePharmAlert.
To fill out MHRA alerts - ePharmAlert, individuals should complete the online reporting form with details of the incident, including product information, the nature of the alert, and any relevant clinical information.
The purpose of MHRA alerts - ePharmAlert is to ensure the safety of medications by promptly communicating significant safety issues, allowing healthcare practitioners to take necessary actions to protect patients.
Information that must be reported on MHRA alerts - ePharmAlert includes the product name, batch number, type of alert, and details of the adverse effects or safety concerns associated with the medication.
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