№ lp_1_36220
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Professional development opportunities for TMD personnel, including both Army and Air Officers, aimed at enhancing their qualifications through various JPME courses and training sessions within the fiscal year 2018.
Year:
2017
Region / City:
Camp Mabry, Austin TX
Topic:
Joint Professional Military Education (JPME) Training Opportunities
Document Type:
Military Training and Education Plan
Organization / Institution:
JFHQ-Texas
Author:
N/A
Target Audience:
TMD NCOs and Officers, Army and Air Officers
Period of Validity:
FY18
Approval Date:
N/A
Date of Modifications:
N/A
Price: 8 / 10 USD
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The file will be delivered to the email address provided at checkout within 12 hours.
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The product description is provided for reference. Actual content and formatting may differ slightly.
Note:
Year
Subject:
Colour Reference Copies, Product Colors, Standardization
Document Type:
Order Form
Organization / Institution:
Husqvarna Group
Target Audience:
Suppliers, Manufacturers
Year:
N/A
Region / city:
N/A
Topic:
miR-122, hepatocyte cultures, acetaminophen, diclofenac, cytotoxicity
Document type:
Supplementary figure
Author:
N/A
Target audience:
Researchers in the field of hepatology, toxicology, and molecular biology
Period of validity:
N/A
Date of approval:
N/A
Date of amendments:
N/A
Year:
2025
Region / City:
Washington, D.C.
Subject:
Copyright law, digital performance, sound recordings
Document Type:
Legal Order
Organization:
United States Copyright Royalty Judges
Author:
United States Copyright Royalty Judges
Target Audience:
Legal professionals, copyright law practitioners, entities involved in music licensing
Period of Effect:
2025-2026
Approval Date:
April 8, 2025
Date of Amendments:
Not specified
Document No:
FDA/DNC/TEM-04
Year:
2024
Region / City:
Accra, Ghana
Theme:
Immunological Veterinary Medicinal Products
Document Type:
Guideline
Organization:
Food and Drugs Authority
Author:
World Health Organization
Target Audience:
Applicants and Manufacturers of Pharmaceutical Products
Approval Date:
1st April 2019
Date of Issue:
8th January 2024
Changes Date:
N/A
Note:
Year
Region / City:
Victoria
Subject:
Co-operatives
Document Type:
Form
Authority:
Consumer Affairs Victoria
Year:
2014
Region / City:
Texas
Subject:
Filing Procedures, Motions, Court Practices
Document Type:
Court Procedure Guidelines
Agency / Institution:
Texas Supreme Court
Author:
Texas Court System
Target Audience:
Legal Professionals
Effective Period:
From January 1, 2014
Approval Date:
January 1, 2014
Year:
2024
Region / City:
Accra, Ghana
Theme:
Pharmaceutical Labelling
Document Type:
Guideline
Organization / Institution:
Food and Drugs Authority
Author:
Food and Drugs Authority
Target Audience:
Pharmaceutical Manufacturers
Validity Period:
Ongoing
Approval Date:
1st February 2013
Date of Revision:
8th January 2024
Year:
2017
Region / City:
United States
Topic:
Immigration Law, U-visa cases, Criminal Law
Document Type:
Memorandum
Organization / Institution:
Sanctuary for Families
Author:
Not specified
Target Audience:
Legal professionals, Immigration attorneys
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Document Type:
Form
Institution:
Indian Institute of Technology Indore
Target Audience:
Postgraduate students
Year:
2023
Region / City:
Kent
Topic:
Local wildlife sites, roadside nature reserves
Document Type:
Request form
Organization / Institution:
Kent Wildlife Trust
Author:
Kent Wildlife Trust
Target Audience:
General public, organizations needing site information
Action Period:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Region / City:
Washington, D.C.
Subject:
Land Entry Files Request
Document Type:
Order Form
Authority / Institution:
National Archives and Records Administration (NARA)
Author:
National Archives and Records Administration
Target Audience:
Researchers, individuals seeking land entry files
Year:
2023
Region / City:
Fort Myers, Florida
Topic:
Legal Procedure
Document Type:
Court Notice
Agency / Institution:
United States District Court
Author:
Deputy Clerk
Target Audience:
Pro se litigants, attorneys
Period of Validity:
N/A
Approval Date:
[DATE]
Date of Changes:
N/A
Contextual Description:
A court-issued notice detailing procedural steps for filing motions related to summary judgment in a case, including deadlines for responses and evidence submission.
Note:
Year
Theme:
Research Protocol
Document Type:
Research Protocol
Year:
2012
Date Range:
15–19 January 2012
Volume:
58
Compiler:
Dr Umar Azam
Archive:
Archive of Dr Umar Azam
Place of Compilation:
Manchester, UK
Subject:
Requests for digital copies of the Holy Quran and related Islamic e-books
Document Type:
Email correspondence archive
Languages Mentioned:
Arabic, Urdu, English
Related Works:
Holy Quran; Aab-e-Kausar Book of Durood Duas; Power of Durood Sharif; Hajj E-Book; Duas E-Book
Correspondents:
Various individual email senders
Medium:
Electronic mail
Document type:
Contract management plan
Date:
Thursday, June 21, 2018
Organisation:
NSW Procurement
Region:
New South Wales, Australia
Intended parties:
NSW Procurement and suppliers
Contract governance scope:
Operational and strategic
Subject area:
Public procurement and contract governance
Document status:
Supplier copy
Approval responsibility:
NSW Procurement Category Manager and Supplier Account Manager
Record retention period:
Contract term plus seven years
Audit provisions:
Annual audit and inspections permitted under Head Agreement
Dispute resolution framework:
Escalation levels defined within NSW Procurement and supplier
Insurance requirements:
Public liability, workers compensation, professional indemnity
Liability provisions:
Customer and supplier liability caps defined per customer contract
Year:
2023
Region / city:
N/A
Topic:
Open access publishing, academic books
Document type:
Promotional content
Institution:
JSTOR
Author:
N/A
Target audience:
Authors, researchers, academic staff
Period of validity:
N/A
Approval date:
N/A
Date of changes:
N/A
Note:
Year
Topic:
Certification of True Copy
Document Type:
Application Form
Organization:
The Hong Kong Polytechnic University
Target Audience:
Students of The Hong Kong Polytechnic University
Context:
Application form for certifying a true copy of academic documents issued by The Hong Kong Polytechnic University.
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Document No:
FDA/DNC/TEM-01
Year:
2024
Region / City:
Accra, Ghana
Subject:
Immunological Veterinary Medicinal Products
Document Type:
Guideline
Organization / Institution:
Food and Drugs Authority
Author:
Food and Drugs Authority
Target Audience:
Pharmaceutical manufacturers, regulatory authorities
Validity Period:
Not specified
Approval Date:
1st February 2013
Revision Date:
30th January 2024