NLM Digital Collections

Search

Start Over Subjects Documentation -- standards ✖Remove constraint Subjects: Documentation -- standards Publication Year 2000 to 2023 ✖Remove constraint Publication Year: <span class="from" data-blrl-begin="2000">2000</span> to <span class="to" data-blrl-end="2023">2023</span>

1. Center for Devices and Radiological Health appeals processes: questions and answers about 517A : guidance for industry and Food and Drug Administration staff

Publication:
[Silver Spring, Maryland] : Center for Devices and Radiological Health, September 29, 2017
Subject(s):
Device Approval -- standards
Documentation -- standards
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
United States.

2. Developing and responding to deficiencies in accordance with the least burdensome provisions: guidance for industry and Food and Drug Administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, September 29, 2017
Subject(s):
Device Approval -- standards
Communication
Documentation -- standards
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

3. M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use

Publication:
Silver Spring, MD : Center for Drug Evaluation and Research, October 2017
Subject(s):
Documentation -- standards
Drug Approval
Congresses as Topic
European Union
International Cooperation
Pharmaceutical Preparations -- standards
Humans
Canada
Europe
Japan
Switzerland
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

4. Standardizing reporting of patient falls: a survey of Pennsylvania hospitals

Publication:
[Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, c2012
Subject(s):
Accidental Falls -- prevention & control
Accidental Falls -- statistics & numerical data
Documentation -- standards
Interinstitutional Relations
Mandatory Reporting
Regional Medical Programs -- organization & administration
Data Collection -- methods
Health Care Surveys
Hospitals
Humans
Pennsylvania
United States

5. Health document submission requirements for tobacco products: (revised)

Publication:
Silver Spring, MD : Center for Tobacco Products, October 2017
Subject(s):
Documentation -- standards
Tobacco Products -- standards
Drug Approval
Health
Terminology as Topic
Tobacco Products -- adverse effects
Tobacco Products -- toxicity
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
United States.

6. Falls rates improved in Southeastern Pennsylvania: the impact of a regional initiative to standardize falls reporting

Publication:
[Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, c2012
Subject(s):
Accidental Falls -- prevention & control
Accidental Falls -- statistics & numerical data
Documentation -- standards
Interinstitutional Relations
Mandatory Reporting
Patient safety
Regional Medical Programs -- organization & administration
Aged
Data Collection -- methods
Drug-Related Side Effects and Adverse Reactions
Health Care Surveys
Hospitals
Risk Assessment
Humans
Pennsylvania
United States