Ad
related to: clinical governance in pharmacy explained
Search results
Results From The WOW.Com Content Network
Clinical governance is a systematic approach to maintaining and improving the quality of patient care within the National Health Service (NHS) and private sector health care. Clinical governance became important in health care after the Bristol heart scandal in 1995, during which an anaesthetist, Dr Stephen Bolsin , exposed the high mortality ...
European Union: In the EU, Good Clinical Practice is backed and regulated by formal legislation contained in the Clinical Trial Regulation (Officially Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC). [3]
The pharmacy services provided are accessible to patients and the public. The services are not provided, and are not accessible to the public, if the pharmacy is closed when the public would reasonably expect it to be open. 4.2 Pharmacy services are managed and delivered safely and effectively. This may not be the case when there are closures.
Swage T.; Clinical governance in health care practice. Oxford: Butterworth-Heinemann, 2000; Clinical Governance Support Team, A Practical Handbook for Clinical Audit. 2004; Clinical governance and re-validation: the role of clinical audit, Education in Pathology. 2002;117:47–50; The New NHS, Modern, Dependable, London: HMSO, 1997, ISBN 0-10 ...
Clinical pharmacy is the branch of pharmacy in which clinical pharmacists provide direct patient care that optimizes the use of medication and promotes health, wellness, and disease prevention. [ 1 ] [ 2 ] Clinical pharmacists care for patients in all health care settings but the clinical pharmacy movement initially began inside hospitals and ...
Arkansas on Monday sued two pharmacy benefit managers that oversee coverage for insurers, employers and other large clients, accusing them of fueling the opioid crisis in the state. Attorney ...
In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.
Clinical quality management systems (CQMS) are systems used in the life sciences sector (primarily in the pharmaceutical, biologics and medical device industries) designed to manage quality management best practices throughout clinical research and clinical study management. A CQMS system is designed to manage all of the documents, activities ...