Description
This assignment is designed to give you a greater understanding of regulatory agencies and accreditation bodies, including their functions, public reporting requirements, and the how they impact quality and safety.
select and evaluate a regulatory agency or accrediting body.
- Discuss the history of the agency or body.
- Explain the reason for its existence.
- Summarize the agency's public reporting of quality indicators:
- Frequency
- Where they are reported
- Why public reporting of these metrics is important
- Explain how the agency or body operates:
- Current function
- Organizational structure
- Governance
- Analyze the impact the agency or body has on quality at each level of health care:
- Health care organizations
- Nursing practice
- Patient care
Cite at least two sources in an APA 7th edition formatted reference page.
Format your assignment as one of the following:
- 875-word paper
- RUBRIC
- Discussed the history of an appropriate regulatory agency or accrediting body and explained the reason for creation or existence.
- Summarized the agency’s public reporting of quality indicators:
- o Frequency
- o Where they are reported
- o Why public reporting of these metrics is important
- Explained how the agency or body operates:
- o Current function o Organizational structure
- o Governance
-
40
Analyzed the impact the agency or body has on quality
at each level of health care:
- o Healthcare organizations
- o Nursing practice
- o Patient care
- Format: points possible Points possible Points earned Comments
- Followed a structure that is clear, concise, and appropriate; maintained a scholarly tone
- Cited at least two sources in an APA-formatted reference page
Explanation & Answer
Please view explanation and answer below.
1
Medical and Healthcare products Regulatory Agency
Your name
Instructor's name
Course
Date of submission
2
Medical and Healthcare products Regulatory Agency
History
It is one of the agencies in the United Kingdom, specifically under the department of
health and social care. The executive agency has the following responsibilities; ensuring that the
medicines and medical equipment perform their work and that the equipment and the drug are
safe for utilizing. The agency was founded in 2003 following a merger between Medicines
Control Agency (MCA) and the Medical Devices Agency (MDA). The agency merged
with National Institute for Biological Standards and Control (NIBSC) in April 2013. In the same
period, the agency was rebranded into Medical and Health care products Regulatory
Agency(MHRA), where the central role of the agency was for the regulatory center within the
group. The agency has a capacity of 1200 employees where some are from London, York, South
Mimms, and Hertfordshire.
Reasons for its existence
The agency aids in operating the post-marketing surveillance. This surveillance is mainly
conducted on the drug reactions and issues with medical equipment; thus, the agency conducts
an investigation and monitoring on the above areas of medicine. The agency enhances the safe
use of drugs and devices to promote health among the public (Milne...
