№ files_lp_3_process_7_072630
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This document is a letter outlining the medical necessity for vaginal dilation therapy to treat vaginismus and related conditions.
Year:
[Not specified]
Region / City:
[Not specified]
Theme:
Medical necessity
Document Type:
Medical letter
Organization / Institution:
[Not specified]
Author:
[Not specified]
Target Audience:
Medical reviewers
Period of validity:
[Not specified]
Approval Date:
[Not specified]
Date of amendments:
[Not specified]
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2015
Institution:
Rice University
Type of document:
Educational textbook chapter
Subject:
Physics, Special Relativity
Target audience:
AP® course students
Topics covered:
Time dilation, length contraction, relativistic momentum, relativistic energy, relativistic addition of velocities
Chapter:
28
Exercises included:
Yes, with step-by-step solutions
Unit of measurement:
SI units and particle physics units (MeV, s, km)
Year:
2016
Region / City:
USA
Topic:
Labor induction, Obstetrics, Coding Guidelines
Document Type:
Guidelines
Organization:
American College of Obstetricians and Gynecologists (ACOG)
Author:
Menard MK, Main EK, Currigan SM
Target Audience:
Medical professionals, Coding staff, Obstetrics departments
Period of validity:
Not specified
Approval Date:
2016-07-15
Date of Changes:
Not specified
Year:
2023
Region / city:
Ireland
Topic:
Healthcare, Medical Devices, Adverse Incidents
Document type:
Guide
Author:
Health Products Regulatory Authority (HPRA)
Target audience:
Healthcare Professionals, National Mesh Administrators
Date of approval:
2023
Date of changes:
N/A
Year:
2023
Region / City:
Kenya
Topic:
Vaginal microbiota, gestational age, preterm birth
Document Type:
Research study
Institution:
University of Nairobi, University of Washington, Kenyatta National Hospital, Coast General Teaching and Referral Hospital, Women’s Healthcare Associates, Fred Hutchinson Cancer Centre, PathCare Laboratories
Author:
R. Scott McClelland, Jackson Nyangaresi, Erica M Lokken, Sujatha Srinivasan, John Kinuthia, Barbra A Richardson, Hudson Alumera, Sophia M R Lannon, Shahid Hussein, Tina Fiedler, Anne Pulei, Matthew Munch, Arthur Kemoli, Sean Proll, Kishorchandra N Mandaliya, Grace John-Stewart, Walter Jaoko, David N Fredricks
Target Audience:
Researchers, healthcare professionals
Period of validity:
April 2017 – December 2020
Date of approval:
Not stated
Date of changes:
Not stated
Year:
2026
Region / City:
Tennessee, USA
Theme:
Obstetrics, Maternal Health, Cesarean Birth Reduction
Document Type:
Quality Improvement Protocol
Organization / Institution:
Tennessee Department of Health, TIPQC
Author:
Danielle Tate, MD, MFM; Connie Graves, MD, MFM; Bonnie Miller, MSN, RN; Brenda Barker, MEd, MBA; Theresa Scott, MS; Rolanda Lister, MD
Target Audience:
Healthcare providers, obstetric care teams, hospital administrators
Period of Validity:
Ongoing
Approval Date:
2026
Modification Date:
Not specified
Year:
2026
Region / City:
Chandigarh, India
Subject:
Vaginal contraception, microbiology
Document Type:
Research article
Institution:
Panjab University, Department of Microbiology
Author:
Siftjit Kaur, Vijay Prabha
Target Audience:
Researchers, healthcare professionals
Experimental Model:
Female BALB/c mice
Methodology:
Isolation, characterization, and in-vitro/in-vivo testing of sperm-agglutinating factor (SAF)
Safety Evaluation:
Vaginal epithelium integrity, reproductive performance, systemic toxicity
Number of Published Articles by Author:
111
Contact Email:
[email protected]
Alternative Email:
[email protected]
Phone Number:
+91 9417065675
Note:
Year
Theme:
Medical Equipment, Adaptive Devices
Document Type:
Medical Necessity Letter
Target Audience:
Insurance Providers, Medical Professionals
Organization:
Driscoll Health Plan
Document type:
Clinical policy and administrative guidelines
Revision date:
November 1, 2024
Geographic scope:
Texas
Programs referenced:
STAR, STAR Kids, CHIP
Subject area:
Therapy services prior authorization and medical necessity
Target audience:
Therapy providers and referring physicians
Authorization method:
Provider web portal and fax submission
Related forms:
Texas Standard Prior Authorization Request Form for Health Care Services (TARF), Therapy Referral Review by Ordering Physician Attestation Form
Effective policy elements:
Initial evaluations, re-evaluations, continuation of therapy, start of care rules
Coverage criteria:
Medical necessity based on clinical documentation
Source type:
Health plan policy guideline
Year:
2021
Region / City:
United States
Topic:
Medical Necessity Letter, Health Treatment
Document Type:
Medical Document
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Medical professionals, healthcare providers
Period of validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2021
Region / City:
California, Arizona
Topic:
Energy Transmission, Public Utilities
Document Type:
Decision
Organization / Institution:
California Public Utilities Commission
Author:
California Public Utilities Commission
Target Audience:
Stakeholders in energy infrastructure and transmission
Effective Period:
N/A
Approval Date:
November 4, 2021
Date of Changes:
N/A
Year:
2025
Region / City:
United States
Theme:
Medical necessity letter
Document type:
Medical letter
Organization / Institution:
Takeda Pharmaceuticals U.S.A., Inc.
Author:
Takeda Pharmaceuticals U.S.A., Inc.
Target audience:
Physicians, insurance providers
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Note:
Date
Diagnosis:
G36.0, neuromyelitis optica [Devic]
Treatment:
UPLIZNA® (inebilizumab-cdon), injection, 1 mg
Reason for request:
Medical necessity for treatment of neuromyelitis optica spectrum disorder (NMOSD) with UPLIZNA
Enclosures:
Prescribing Information, clinical notes, FDA approval letter, patient relapse history, test results, etc.
Year:
2024
Region / City:
United States
Topic:
Medical Necessity Letter
Document Type:
Medical Letter
Organization / Institution:
Bausch + Lomb
Author:
Physician
Target Audience:
Healthcare providers, Payers
Action Period:
June 2024
Approval Date:
June 2024
Modification Date:
N/A
Document type:
Medical necessity letter
Therapeutic area:
Ophthalmology
Indication:
Reduction of intraocular pressure in open-angle glaucoma or ocular hypertension
Medication name:
VYZULTA (latanoprostene bunod ophthalmic solution)
Dosage strength:
0.024%
Drug class:
Prostaglandin analogue with nitric oxide–donating activity
Regulatory status:
FDA-approved prescription medication
Manufacturer:
Bausch & Lomb Inc.
Intended recipient:
Health insurance payer or medical director
Target population:
Patients with open-angle glaucoma or ocular hypertension
Clinical evidence referenced:
Phase 2 VOYAGER study; Phase 3 APOLLO and LUNAR studies; real-world retrospective studies
Safety information included:
Yes
References:
Peer-reviewed journals and prescribing information
Source type:
Industry-provided informational material
Year:
2025
Region / City:
Princeton, NJ
Theme:
Medical necessity documentation
Document Type:
Medical letter
Organization / Institution:
Bristol-Myers Squibb Company
Author:
<>
Target Audience:
Healthcare professionals, physicians
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2025
Jurisdiction:
West Virginia, United States
Type of document:
Legislative Act
Governing body:
West Virginia Legislature
Authors:
Delegates Riley, Linville, D. Cannon, Eldridge
Effective date:
April 11, 2025
Subject:
Public utilities regulation, water and sewer services, certificate of public convenience and necessity
Legal references:
§24-2-11, §31-15A-1 et seq. of the West Virginia Code
Scope:
Construction projects of water and sewer services for utilities with at least 4,500 customers and $3 million or more in annual revenues
Approval authority:
Public Service Commission, Infrastructure and Jobs Development Council
Decision timelines:
Standard projects 225–270 days, projects >$50 million 400 days
Year:
2023
Region / City:
United States
Subject:
Healthcare
Document Type:
Template
Institution / Organization:
Takeda Oncology
Author:
Takeda Oncology
Target Audience:
Healthcare providers, insurance companies
Effective Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Date
Year:
2026
Region / City:
N/A
Topic:
Genetic Testing, Exome Sequencing
Document Type:
Letter
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Healthcare providers, medical practitioners
Validity Period:
N/A
Approval Date:
N/A
Modification Date:
N/A
Program:
Illinois Early Intervention Program
State:
Illinois
Type of document:
Administrative form
Subject area:
Early intervention services
Focus:
Assistive technology justification
Target population:
Infants and toddlers enrolled in Early Intervention
Associated plan:
Individualized Family Service Plan (IFSP)
Required contributors:
Early Intervention evaluator, service coordinator, physician
Required approvals:
Physician signature
Content sections:
Demographic information, provider information, IFSP details, assessment and justification
Purpose:
Documentation of developmental necessity for assistive technology items