№ lp_1_2_61655
File format: docx
Character count: 6899
File size: 68 KB
The document is a form used by Small Authorised UK AIFMs to provide specific information for authorisation, detailing business intentions, customer data, investment plans, and fund management details.
Note:
Year
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2021
Region / City:
European Union
Topic:
Cross-border marketing of EU AIFs
Document type:
Notification letter
Author:
European Commission
Target audience:
AIFMs, regulatory bodies, financial institutions
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Note:
Year
PART 1:
Information on the AIFM or internally managed AIF
PART 2:
Information on the AIFs to be marketed in the host Member State
Year:
2011
Jurisdiction:
European Union
Legal Basis:
Directive 2011/61/EU, Article 33(2) and Article 33(3)
Subject:
Cross-border management of alternative investment funds and establishment of branches
Document Type:
Regulatory notification form
Issuing Framework:
Directive 2011/61/EU of the European Parliament and of the Council
Addressee:
Competent authority of the AIFM home Member State
Applicant:
EU Alternative Investment Fund Manager (AIFM)
Scope:
Management of EU AIFs in host Member States or establishment of a branch
Referenced Legislation:
Directive (EU) 2016/2341
Structure:
Part 1 (Information on the AIFM); Part 2 (Freedom to provide services); Part 3 (Establishment of a branch)
Required Information:
Identification data, programme of operations, information on AIFs, branch details, delegation arrangements, master-feeder structures
Note:
Year
Authority / institution:
Central Bank
Description of the operational programme:
Includes procedures and governance details for managing EU AIFs in another member state, focusing on regulatory compliance and cross-border services.
Year:
2022
Region / City:
Not specified
Subject:
Nuclear safety, regulatory compliance
Document Type:
Technical Guide
Organization:
Office for Nuclear Regulation (ONR)
Author:
Nuclear Equivalence Inspector
Target Audience:
ONR inspectors, licensees
Period of Validity:
Until Dec-2025
Approval Date:
Dec-2022
Revision Date:
Not specified
Document Reference:
NS-INSP-GD-012
Record Reference No.:
2022/72622
Year:
2017-2020
Region / City:
Ballymount, Dublin
Theme:
Waste Management
Document Type:
Application Form
Organization:
Circol ELT Ltd
Author:
Circol ELT Ltd
Target Audience:
Waste collectors, companies seeking registration
Period of validity:
2017-2020
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Country:
Australia
Type of document:
Application form
Issuing authority:
Therapeutic Goods Administration (TGA)
Intended audience:
Medical practitioners
Purpose:
Application to become an authorised prescriber of unapproved medicines or medical devices
Regulatory reference:
Therapeutic Goods Regulations 1990, Regulation 12B(1B)
Required attachments:
Ethics committee or specialist college approval/declaration (if applicable)
Information collected:
Personal details of medical practitioner, patient consent, product information, prescribing details
Submission method:
Email or fax to TGA
Year:
2024
Region / City:
European Union
Topic:
Vehicle Authorization, Regulatory Changes
Document Type:
Notification Form
Agency:
European Union Agency for Railways
Author:
European Commission
Target Audience:
Entities managing vehicle authorization changes
Period of Validity:
From 1 October 2024
Approval Date:
Not specified
Date of Changes:
1 October 2024
Context:
A notification form used by entities to inform the European Union Agency for Railways about changes to an already authorized vehicle, following regulatory guidelines and requirements for new authorizations under EU regulations.
Year:
2023
Region / City:
European Union
Topic:
Clinical Trials, Medical Regulation
Document Type:
Cover Letter
Organization:
European Commission
Author:
European Commission
Target Audience:
Pharmaceutical Companies, Clinical Trial Sponsors
Action Period:
Transition of Clinical Trials from Directive 2001/20/EC to Regulation (EU) No 536/2014
Approval Date:
N/A
Amendment Date:
N/A
Year:
2015
Type of document:
Assessment report template
Subject:
Pharmacovigilance, Periodic Safety Update Reports (PSUR)
Organization:
European Medicines Agency (EMA)
Target audience:
Lead Member States, MAHs, PRAC members
Procedure number:
Not specified
Data lock point:
Not specified
Status:
Guidance and procedural template
References:
GVP Module V, VII, VIII; Variations Classification guideline Commission Regulation 1234/2008; HMA/EMEA recommendations EMEA/743133/2009
Year:
2023
Region / City:
United Kingdom
Subject:
Medical treatment, Court of Protection
Document Type:
Practice Guidance
Institution:
Court of Protection
Author:
Mr Justice Hayden
Target Audience:
Legal professionals, healthcare providers, commissioners of clinical services
Period of Validity:
Until superseded by revised MCA Code
Approval Date:
Not specified
Date of Amendments:
Not specified
Effective date:
1 August 2006
Document type:
Administrative mandate
Sector:
General Ophthalmic Services
Regulatory framework:
GOS Terms of Service
Subject:
Authorised signatories for GOS1 forms
Jurisdiction:
United Kingdom
Signatory requirements:
Practitioner and Contractor signatures under specified circumstances
Scope:
Financial and regulatory responsibilities for GOS claims
Supersedes:
All previous practice mandates
Change procedure:
New mandate required for any change in signatories
Note:
Date
Year:
2020
Region / City:
Australia
Topic:
Paramedicine
Document Type:
Template
Organization / Institution:
Paramedicine Board of Australia
Author:
Paramedicine Board of Australia
Target Audience:
Paramedics required to undertake supervised practice
Effective Date:
27 November 2020
Period of Supervision:
Varies based on individual plan
Date of Approval:
27 November 2020
Date of Changes:
Not specified
Institution:
University of West London
Department:
Compliance Team
Document Type:
Administrative form
Subject:
Authorised absence during term time
Applicable To:
Student Visa holders
Regulatory Framework:
UK Visas and Immigration regulations
Maximum Approved Period:
Two weeks
Required Evidence:
Documentary evidence (UK registered medical practitioner for health issues)
Approval Process:
Personal Tutor or Course Leader signature and Compliance Team approval
Submission Method:
Email to [email protected]
Related Authority:
UK Border Agency