Author:
Publisher:
ISBN:
Category : Physicians
Languages : en
Pages : 420
Book Description
The Medical Register
Author:
Publisher:
ISBN:
Category : Physicians
Languages : en
Pages : 420
Book Description
Publisher:
ISBN:
Category : Physicians
Languages : en
Pages : 420
Book Description
Polk's Medical Register and Directory of the United States and Canada
Author:
Publisher:
ISBN:
Category : Physicians
Languages : en
Pages : 2548
Book Description
Publisher:
ISBN:
Category : Physicians
Languages : en
Pages : 2548
Book Description
The Medical Register and Directory of the Practitioners of Medicine, in the City and County of Philadelphia
Author: Samuel B. Hoppin
Publisher: BoD – Books on Demand
ISBN: 3385461391
Category :
Languages : en
Pages : 78
Book Description
Publisher: BoD – Books on Demand
ISBN: 3385461391
Category :
Languages : en
Pages : 78
Book Description
Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
Book Description
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
Book Description
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
The Indian Medical Council Act, 1956
Author:
Publisher: Universal Law Publishing
ISBN:
Category :
Languages : en
Pages : 192
Book Description
Publisher: Universal Law Publishing
ISBN:
Category :
Languages : en
Pages : 192
Book Description
Minutes of the General Medical Council, of Its Executive and Dental Committees, and of Its Branch Councils
Author: General Medical Council (Great Britain)
Publisher:
ISBN:
Category :
Languages : en
Pages : 466
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 466
Book Description
Annual Report of the Indiana State Board of Medical Registration and Examination
Author: Indiana. State Board of Medical Registration and Examination
Publisher:
ISBN:
Category : Medical laws and legislation
Languages : en
Pages : 324
Book Description
Publisher:
ISBN:
Category : Medical laws and legislation
Languages : en
Pages : 324
Book Description
The Canada Medical Record
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 682
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 682
Book Description
Annual report of the Indiana State Board of Medical Registration and Examination. 1911
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 380
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 380
Book Description
Medical Record
Author:
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 760
Book Description
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 760
Book Description