№ files_lp_4_process_2_69892
File format: docx
Character count: 291
File size: 25 KB
Provides structured information on gap-filling modules, including course names, institutions, duration, module codes, and contact hours, for educational reference.
Year:
2026
Region / City:
Not specified
Subject:
Education, Diploma bridging programmes
Document Type:
Annexure
Institution:
Not specified
Target Audience:
Diploma holders seeking lateral entry
Programme Duration:
Not specified
Number of Modules:
Not specified
Module Codes:
Provided
Module Names:
Provided
Contact Hours:
Provided
Non-Contact Hours:
Provided
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
Not specified
Location:
Los Angeles, USA
Theme:
Traffic incident / Driving behavior
Document type:
Educational listening exercise
Institution:
Language learning center
Target audience:
English language learners
Skills focused:
Listening comprehension, vocabulary
Characters:
Graham, officer, unnamed drivers
Situation:
Car accident and interaction with law enforcement
Format:
Script with fill-in-the-blank activity
Language:
English
Level:
Intermediate ESL
Year:
2025
Region / City:
United Kingdom
Topic:
COVID-19 treatment, lateral flow device tests
Document Type:
Service Specification
Organization / Institution:
NHS England
Author:
NHS England
Target Audience:
Pharmacy contractors, healthcare professionals
Period of Validity:
Ongoing, from 6 November 2023
Date of Approval:
May 2025
Date of Changes:
01 May 2025
Year:
2023
Region / Country:
Australia
Drug:
Edaravone (Radicava®)
Type of Document:
Pharmaceutical Benefits Submission
Regulatory Body:
Therapeutic Goods Administration (TGA)
Submission Purpose:
PBS Section 100 Highly Specialised Drugs Listing
Indication:
Amyotrophic lateral sclerosis (ALS)
Treatment Phase:
Initial and Continuing treatment
Prescriber Type:
Medical Practitioners, Nurse Practitioners (continuing therapy only)
Clinical Criteria:
Diagnosis by neurologist, disease duration ≤ 2 years, FVC or SVC ≥ 80% predicted, ambulatory or upper limb/swallowing ability, ALSFRS-R ≥ 2 on each item, no tracheostomy or respiratory failure
Population:
Adult patients (≥18 years)
Pricing:
Special Pricing Arrangements apply
Regulatory Dates:
Orphan designation 17 August 2021, TGA registration 15 February 2023
Comparator:
Standard of care with or without riluzole
Outcomes Measured:
ALS Functional Rating Scale – Revised (ALSFRS-R) after 6 months
Year:
2023
Note:
Region/City
Topic:
Legal Recruitment
Document Type:
Questionnaire
Organization/Institution:
NALSC®
Author:
NALSC®
Target Audience:
Legal professionals, law firms, recruiters
Year:
Not specified
Region / City:
Not specified
Topic:
Military application
Document Type:
Instructions
Organization / Institution:
Australian Defence Force
Author:
Not specified
Target Audience:
Applicants to the Australian Defence Force
Period of Validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Year of Discovery:
1870s
Location of Discovery:
Paris, France
Medical Field:
Neurology
Document Type:
Informational article
Author:
Samantha Budge
Target Audience:
General public, students of human biology
Affected Population:
Mostly active adults
Symptoms:
Muscle weakness, poor balance, speech and swallowing difficulties, fatigue
Progression:
Loss of mobility, respiratory support needed, dietary adjustments
Life Expectancy:
Typically 2–8 years, occasionally over 10 years
Treatment Approaches:
Medications for spasms and cramps, physical therapy, rest, dietary management
Year:
2023
Region / City:
Manado
Topic:
Medical Rehabilitation
Document Type:
Case Report
Institution:
RSUP Kandou Manado
Author:
Natalia Nanlohy, Joudy Gessal, Christina Adelle Damopolii
Target Audience:
Medical professionals, researchers
Duration:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2018-2021
Note:
Region / City
Subject:
Master of Computer Applications Program Structure
Document Type:
Academic Program
Institution:
School of Engineering
Target Audience:
Students of MCA Program
Period of Validity:
2018-2021
Year:
2021
Region / City:
Zhejiang Province, China
Topic:
Epilepsy, Neuroscience
Document Type:
Research Article
Organization / Institution:
Zhejiang University
Author:
Lin Zhou, Liang Zhou, Li-Da Su, Sheng-Long Cao, Ya-Jun Xie, Ying Shen
Target Audience:
Researchers in neuroscience and epilepsy
Period of Action:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2023
Region / City:
Utsunomiya, Japan
Subject:
Digital Holography, Industrial Measurement
Document Type:
Research Paper
Institution:
Utsunomiya University, Center for Optical Research and Education (CORE)
Author:
Yuma Sato, Yoshio Hayasaki
Target Audience:
Researchers, Engineers in Optical Measurement
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2019
Region / City:
Not specified
Topic:
Patient-reported outcome measures in hip disorders
Document Type:
Systematic review
Author:
Beck et al.
Target Audience:
Healthcare professionals, researchers in orthopedics
Period of Action:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Condition:
Tennis Elbow (Lateral Elbow Tendinopathy)
Alternative names:
Lateral epicondylitis
Type of document:
Patient information leaflet
Medical field:
Musculoskeletal health
Affected area:
Elbow and forearm
Common age range:
40–60 years
Prevalence:
Up to 1 in 3 people during lifetime
Primary symptoms:
Lateral elbow pain radiating to forearm and wrist
Common causes:
Repetitive wrist extension, gripping and forearm overuse
Diagnostic method:
Clinical assessment and physical examination
Imaging:
Ultrasound or other imaging if nerve damage suspected
Conservative management:
Activity modification, exercise therapy, ice application, support strap, analgesia
Recovery duration:
6 months to 2 years
Rehabilitation response time:
Up to 12 weeks
Referral options:
Physiotherapy, shockwave therapy, steroid injection, surgery
Lifestyle considerations:
Stress management, sleep, alcohol avoidance, smoking cessation, physical activity
Target audience:
Patients experiencing lateral elbow pain
Year:
2024
Country:
Nigeria
State:
Nasarawa State
City / Area:
Keffi
Institution:
Federal Medical Centre Keffi
Department:
Medical Laboratory Department, Blood Bank
Document Type:
Original Research Article
Study Design:
Cross-sectional study
Study Period:
March 2024 – September 2024
Sample Size:
240 blood donors
Population:
Blood donors aged 18–65 years meeting eligibility criteria
Research Focus:
Viral transfusion-transmissible infections (HIV, HBV, HCV)
Diagnostic Methods:
Rapid Diagnostic Test (RDT), Enzyme-Linked Immunosorbent Assay (ELISA)
Primary Outcome:
Seroprevalence of transfusion-transmissible viral infections among blood donors
Keywords:
Blood Donors, Enzyme-linked Immunosorbent Assay (ELISA), Rapid Diagnostic Test (RDT), Transfusion-Transmissible Infections (TTIs), Nasarawa
Year:
2021
Institution:
University of Washington
Department:
University of Washington Police Department (UWPD)
City:
Seattle
State:
Washington
Country:
United States
Document type:
Job vacancy announcement
Position title:
Campus Police Officer (Lateral)
Posting date:
February 4, 2021
Closing date:
March 7, 2021
Work location:
Seattle Campus
Salary range:
$5,799–$7,611 per month
Union position:
Yes
Work shift:
First shift (varies by assignment)
Number of openings:
Multiple openings
Employment category:
Law enforcement personnel
Selection process:
Oral board interview, writing exam, ride-along, background investigation, polygraph, medical and psychological examination
Jurisdiction:
University of Washington main campus and surrounding areas
Accreditation references:
CALEA, IACLEA, Washington Association of Sheriffs & Police Chiefs
Year:
Not provided
Region / City:
Not provided
Topic:
Statistical analysis, segmentation, CBCT, MRI, cephalometry
Document Type:
Research article
Organization / Institution:
Not provided
Author:
Abkai et al, Juerchott et al, Jency et al, Grandoch et al, Maspero et al, Heil et al, Eley et al, Tai et al
Target Audience:
Researchers, clinicians, medical imaging specialists
Period of validity:
Not provided
Approval Date:
Not provided
Date of Changes:
Not provided
Context:
Research article evaluating the level of agreement between different imaging modalities (CBCT, MRI, cephalogram) using various statistical methods.
Year:
2017
Region / City:
United States
Topic:
Financial reporting, regulatory filings
Document Type:
Report
Agency / Organization:
Federal Reserve System, FDIC, Office of the Comptroller of the Currency
Author:
Not specified
Target Audience:
Individuals filing regulatory reports
Period of validity:
Not specified
Approval expiration date:
September 30, 2013, April 30, 2014, November 30, 2013
Date of approval:
Not specified
Date of changes:
June 7, 2017
Note:
Date of Application
Financing Amount Required:
RM
Bank Charges:
AmBank Islamic Berhad Charges Paid By Us. Please Debit Our Account No.:
Year:
2016
Region / City:
Malaysia
Subject:
Islamic Banking, Export/Import Financing
Document Type:
Application Form
Organization:
AmBank Islamic Berhad
Author:
AmBank Islamic Berhad
Target Audience:
Businesses involved in export/import transactions
Period of Validity:
N/A
Approval Date:
N/A
Modification Date:
N/A
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.