№ files_lp_3_process_7_045629
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The document is a response form for a public consultation regarding the reservation of water abstraction rights.
Year:
2026
Region / city:
United Kingdom
Topic:
Water Resources Management
Document type:
Consultation response form
Organization:
Environment Agency
Author:
Environment Agency
Target audience:
General public, organizations, and stakeholders
Effective period:
Until February 16, 2026
Approval date:
N/A
Amendment date:
N/A
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Note:
Year
Topic:
Medical data abstraction
Document Type:
Instructional guidelines
Institution:
Hospitals
Target Audience:
Medical professionals
Context:
Instructional document for data abstraction related to term newborns for medical record documentation.
Year:
2007
Region / City:
California
Topic:
Maternal health, pregnancy-associated mortality and morbidity
Document Type:
Review Form
Organization / Institution:
California Pregnancy-Associated Mortality Review (CA-PAMR), California Department of Public Health, Maternal, Child and Adolescent Health Division
Author:
Geller SE, Adams MG, Kominiarek MA, Hibbard JU, Endres LK, Cox SM, Kilpatrick SJ
Target Audience:
Healthcare professionals, maternal health reviewers
Effective Period:
Ongoing
Approval Date:
Not specified
Date of Last Modification:
Not specified
Year:
2026
Region / City:
United Kingdom
Theme:
Water Management, Environmental Protection
Document Type:
Regulatory Position Statement
Agency:
Environment Agency
Author:
Environment Agency
Target Audience:
Stakeholders in water abstraction activities, environmental agencies, and water management professionals
Effective Period:
From 10 February 2026 to 24 March 2026
Approval Date:
10 February 2026
Revision Date:
24 March 2026
Topic:
Reserving risk assessment
Industry:
Health insurance
Document type:
Regulatory guidance and assessment procedures
Primary focus:
Insurance reserves and actuarial opinion review
Key components:
Reserve valuation, reserve adequacy, actuarial standards compliance
Referenced filings:
Statement of Actuarial Opinion, Annual Financial Statement
Regulatory context:
State insurance department financial analysis
Responsible roles:
Analysts, appointed actuaries, supervisors
Applicable standards:
Actuarial Standards of Practice, Health Annual Financial Statement Instructions
Lines of business:
Health insurance
Intended audience:
Insurance financial analysts and regulators
Source type:
Supervisory and analytical guidance
Institution:
Cass Business School
Programme:
MSc Actuarial Management
Module Code:
SMM036
Exam Title:
General Insurance – Reserving & Capital Modelling
Professional Reference:
Subject SP7 of the Institute and Faculty of Actuaries Examinations
Date:
January 2020
Duration:
3 hours
Number of Questions:
Five
Total Pages:
Seven including title page
Assessment Type:
Written examination
Permitted Calculators:
Casio FX-83 GT+, Casio FX-85 GT+, Casio FX-83 GTX, Casio FX-85 GTX, Casio FX-83 MS, Casio FX-85 MS, Casio FX-83 ES, Casio FX-85 ES
Permitted Materials:
Actuarial tables
Dictionaries Permitted:
No
Removal from Exam Room:
Not permitted
Internal Examiner:
Mr David Hargreaves
External Examiner:
Mr Malcolm Kemp
Division of Marks:
Marks allocated per question and sub-question as indicated
Instructions:
Candidates must answer all questions and begin each question on a new page
Year:
2023
Location:
Virginia Tech
Topic:
Laboratory Space Reservation
Document Type:
Procedure
Institution:
Virginia Tech
Author:
Christy Lee, Nicolin Girmes-Grieco
Target Audience:
Virginia Tech employees, student organizations with faculty advisor
Period of Validity:
Ongoing
Approval Date:
N/A
Revision Date:
N/A
Note:
Year
Region / City:
Santa Rosa, CA
Theme:
Family Law
Document Type:
Legal Checklist
Organization:
Superior Court of California, County of Sonoma
Target Audience:
Legal professionals, litigants in family law cases
Context:
A legal checklist used by family law clerks to ensure proper documentation for dissolution or domestic partnership cases, including requirements for jurisdiction, child custody, spousal support, and other related forms.
Year:
N/A
Region / City:
Greece
Subject:
Licence Conditions Compliance
Document Type:
Declaration
Organization / Institution:
TAP AG
Author:
N/A
Target Audience:
Potential shippers
Effective Period:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2026
Region / city:
United Kingdom
Topic:
Good Manufacturing Practice, Advanced Therapy Medicinal Products (ATMPs)
Document type:
Consultation response
Organization / institution:
NHS Advanced Therapy Medicinal Products Working Party
Author:
Anne Black
Target audience:
Pharmaceutical professionals, regulatory bodies, academic researchers
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2019
Region / City:
European Union
Topic:
PRIIPs Regulation amendments
Document Type:
Consultation Paper
Institution:
European Supervisory Authorities (ESAs)
Author:
European Supervisory Authorities (ESAs)
Target Audience:
Stakeholders in financial services and investments
Action Period:
16 October 2019 - 13 January 2020
Approval Date:
16 October 2019
Amendment Date:
Not specified
Year:
2026
Region / City:
Greater Manchester
Theme:
Healthcare, Pharmaceutical Recommendations
Document Type:
Report
Institution:
NHS Greater Manchester Medicines Management Group (GMMMG)
Author:
CRG (Clinical Reference Group)
Target Audience:
Healthcare professionals in the NHS
Period of validity:
Until 27th February 2026 (for specific drugs)
Approval Date:
13th January 2026
Date of Changes:
27th February 2026
Cost Impact:
£61,000 per year
Service Implications:
Transfer of prescribing to primary care, potential reduction in specialist service burden
Description:
Recommendations by the Clinical Reference Group (CRG) for the inclusion, continuation, or discontinuation of specific drugs, including azathioprine suspension and sotrovimab, in the Greater Manchester formulary.
Year:
2016
Region / City:
Australia
Topic:
Pharmacy, Medicine Compounding
Document Type:
Consultation Response
Organization:
Pharmaceutical Society of Australia
Author:
Dr Lance Emerson, Chief Executive Officer
Target Audience:
Pharmacists, Pharmacy Regulators
Period of Validity:
Indefinite
Approval Date:
1 February 2016
Date of Amendments:
None
Contextual Description:
Document is a public consultation response discussing terminology issues and proposed updates regarding compounded parenteral medicines, primarily aimed at Australian pharmacists.
Year:
2019
Region / City:
Australia
Topic:
Recency of Practice for Registered Health Practitioners
Document Type:
Consultation Report
Organization / Institution:
National Boards (Aboriginal and Torres Strait Islander Health Practice Board of Australia, Chinese Medicine Board of Australia, Occupational Therapy Board of Australia)
Author:
National Boards
Target Audience:
Registered Health Practitioners
Period of Validity:
2019
Approval Date:
Not specified
Amendment Date:
Not specified
Context:
A consultation report detailing the review of recency of practice (RoP) registration standards for health practitioners in Australia, aiming to establish revised requirements to ensure ongoing professional competence.
Date:
16 October 2019
Organization:
European Supervisory Authorities (ESAs)
Document type:
Response form
Related regulation:
Commission Delegated Regulation (EU) 2017/653
Country/Region:
European Union
Deadline for responses:
13 January 2020
Confidentiality:
Optional, subject to ESAs rules
Respondent:
German Association of Actuaries (DAV)
Activity sector:
Insurance and Pension
Association representation:
Yes
Purpose:
Comments on proposed amendments to PRIIPs KID
Content focus:
Transparency, comparability, and methodology of PRIIPs pre-contractual documents
Source type:
Consultation response
Year:
2019
Region / City:
Europe
Topic:
PRIIPs Regulation, Digital Solutions, KID
Document Type:
Consultation Response
Organization / Institution:
European Supervisory Authorities (ESAs)
Author:
Association Française de la Gestion financière (AFG)
Target Audience:
Financial Industry Stakeholders
Period of Validity:
Until 13 January 2020
Date of Approval:
16 October 2019
Date of Amendments:
Not specified
Year:
2026
Region / City:
United Kingdom
Topic:
Transmission Connection Asset Charging
Document Type:
Consultation Response Proforma
Organ / Institution:
NESO
Author:
Not specified
Target Audience:
Industry parties
Period of validity:
Until 18 February 2026
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Region/City:
North Carolina
Topic:
NEPA/SEPA Consultation Process for Transportation Projects
Document Type:
Form
Agency/Organization:
North Carolina Department of Transportation (NCDOT)
Author:
NCDOT
Target Audience:
NCDOT staff, project managers, consultants
Period of Validity:
Ongoing, applicable as of the date of approval
Approval Date:
Not specified
Date of Changes:
Not specified
Date:
19 November 2025
Organization:
Medicines, Formulary, and Guidelines Group
Location:
Humber and North Yorkshire, UK
Document type:
Consultation summary / Recommendations
Drug:
MV140 Uromune Sublingual vaccine spray
Indication:
Recurrent lower urinary tract infections in adults
Formulary status:
Red – Specialist urology only
Treatment protocol:
2 sprays sublingually once daily for 3 months, possible rechallenge after 18 months
Cost per patient:
£297.50
Monitoring:
Telephone reviews at 1, 3, 6, 9, 12 months; Consultant Urologist review at 6 and 12 months
Professional target audience:
NHS healthcare professionals
Source:
HNY APC Professional Secretariat, Regional Drug and Therapeutics Centre
Year:
2025
Region / City:
United Kingdom
Subject:
Electricity Regulation, Charging Methodology
Document Type:
Consultation Response Form
Organization:
NESO
Author:
Not specified
Target Audience:
Industry parties, Transmission System Operators, Energy Sector Stakeholders
Validity Period:
From 1st April 2026
Approval Date:
Not specified
Amendment Date:
Not specified