№ lp_2_3_26267
File format: docx Character count: 27773 File size: 37 KB
A set of conditions detailing how data from the Register of Powers of Attorney can be accessed via the RC_BROKER web service, outlining service types, access criteria, and data formats.
Note: Year
Organization / institution: State Enterprise Centre of Registers
Data provision tool: RC_BROKER web service
Service type: Register of Powers of Attorney
Access type: Full information
Link: Link to the input and output XSD schemes
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
ONR Technical Inspection Guide Licence Condition 12 – Duly authorised and other suitably qualified and experienced persons
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
APPLICATION FOR REGISTRATION AS AN AUTHORISED WASTE COLLECTOR
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
Authorised Prescriber Scheme – Application form for unapproved therapeutic goods in Australia
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
NOTIFICATION OF CHANGE TO AN ALREADY AUTHORISED VEHICLE PURSUANT TO ARTICLE 16(4) OF COMMISSION IMPLEMENTING REGULATION (EU) 2018/545
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.
General information on the tenderer or on the company authorised to represent a candidate/bidding consortium
Note: Year
FIT AND PROPER DECLARATION – MB/ LSIsupporting new management body and authorised management applications submitted by Less Significant Institutions (LSI) Appointee’s declaration
Note: Year
Cover letter for the transition of Clinical Trial authorised under Directive 2001/20/EC to Clinical Trial Regulation (EU) No 536/2014
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
Pharmacovigilance Risk Assessment Committee (PRAC) PSUR assessment report template and guidance for nationally authorised medicinal products
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
APPLICATIONS RELATING TO MEDICAL TREATMENT: GUIDANCE AUTHORISED BY THE HONOURABLE MR JUSTICE HAYDEN, THE VICE PRESIDENT OF THE COURT OF PROTECTION
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
APPLICATION FOR REGISTRATION AS AN AUTHORISED WASTE COLLECTOR
Note: Year
Ophthalmic Nominated Authorised Signatory Mandate (from 1 August 2006)
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
LIST OF AUTHORISED SIGNATORIES
Note: Date
Application for Authorisation Supplement for Small Authorised UK AIFM
Note: Year
Supervised practice plan for Authorised Bodies
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
Authorised Absence Request Form During Term Time (Student Visa Holders)
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
Topics: REQUESTUSING RCBROKER authorised