Regulatory directives - PowerPoint PPT Presentation


Evolution of Anti-Money Laundering Regulations in the EU

Explore the history and milestones of Anti-Money Laundering (AML) regulations in the EU, from the initial directives in 1991 to the latest amendments. Learn about the obligations on private entities, enforcement of AML laws, and the focus on gatekeepers in the financial system. The directives have e

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Streamlining Business Licensing in Sarawak through Regulatory Experimentation

This initiative in Sarawak focuses on simplifying the business licensing process through regulatory experiments aimed at reducing regulatory burdens and improving the overall business ecosystem. By implementing innovative strategies such as risk-based approvals and composite licenses, the goal is to

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Understanding POLST and Advance Directives in Healthcare Decision-Making

POLST, or Practitioner Orders for Life-Sustaining Treatment, is a healthcare planning tool that empowers individuals to articulate their medical preferences when facing advanced illness. Contrasting with Advance Directives, which are statements of patient intentions, POLST represents actionable medi

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Overview of EU Criminal Law: Classes, Exam, and Directives

This content provides detailed information on substantive and procedural aspects of EU Criminal Law, covering classes, terms of participation, exam details, and specific directives. It includes guidelines on passing the classes through active participation, presentations, and exams. The schedule out

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Regulatory Update Highlights and Priorities for ONR NGO Forum 2023

The Regulatory Update presented by Mark Foy, Chief Executive, and Chief Nuclear Inspector at the ONR NGO Forum highlighted key areas of focus including ethics, future strategies, and regulatory advancements in the nuclear industry. The forum also featured insights from Donald Urquhart, Executive Dir

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University of Florida Cost Comparisons Directives

The University of Florida has established directives for cost comparisons related to business travel expenses. These guidelines ensure that the university is not paying for costs unrelated to official business. University travelers are required to obtain cost comparisons for upgrades, convenience, a

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Overview of Non-Profit Organisations Bill and Historical Background in Ghana

The article provides an in-depth overview of the Non-Profit Organisations (NPO) Bill in Ghana, highlighting its importance as a tool for development. It covers the challenges faced in the past regarding NPO regulation and outlines the historical background leading to the creation of the NPO Secretar

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Participation of Distributed Energy Resource Aggregations in Wholesale Markets: Compliance with Order No. 2222

The presentation outlines the high-level market design approach by ISO New England to comply with Order No. 2222, allowing distributed energy resources to provide wholesale services. It covers compliance directives, participation models, metering requirements, registration coordination, operational

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Developing an Effective Regulatory Experience Feedback Program for Safety: A Guide for Regulatory Bodies

This Safety Guide aims to assist regulatory bodies in managing regulatory experience by identifying sources, establishing means for information exchange, and implementing record-keeping processes. It addresses the need for cooperation and knowledge sharing among regulatory bodies to enhance safety s

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Current Standards Process for Reliability, Resilience, and Security

The current standards process focuses on ensuring reliability, resilience, and security in regulatory directives. It involves remanding standards to committees, convening technical conferences, re-ballingoting within 45 days, and considering input for further work. The process also covers the initia

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Clear Criteria for Assessing Regulatory-Grade Real-World Data Sources

The discussion at the ISPOR Annual Meeting focused on defining regulatory-grade real-world data (RWD) sources as those of adequate quality for specific regulatory purposes. Panelists emphasized the importance of authenticity, transparency, accuracy, and track record in evaluating data quality. They

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Understanding Assembler Directives and Symbols in Assembly Language

Assembly language is a low-level programming language used for computers, microprocessors, microcontrollers, and ICs. It consists of instructions and directives (pseudo instructions). Assembler directives are statements that guide the assembler during the assembly process. Categories of directives i

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Introduction to 8086 Assembly Language Programming

Assembler directives play a crucial role in guiding the assembly process for 8086 assembly language programming. They dictate how operands are handled, memory organization, and more. This content covers essential directives such as ASSUME, DB, DW, DD, DQ, and DT, providing syntax examples and explan

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Understanding the Regulatory Environment: A Comprehensive Overview

This session delves into the regulatory landscape focusing on the objectives, types, and origins of regulations in the financial sector, particularly in Nigeria. It discusses the essential role of regulation in promoting compliance, protecting stakeholders, and maintaining operational integrity with

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Understanding Regulatory Enzymes in Biochemical Pathways

Regulatory enzymes play a crucial role in controlling the activity of biochemical pathways by responding to the presence of specific molecules. They regulate the pathway's activity, ensuring that products are produced in the required amounts at different times. This article delves into the significa

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Overview of Pipeline Safety Regulatory Updates

The Protecting our Infrastructure of Pipelines and Enhancing Safety Act of 2016 authorizes funding for PHMSA. Information on rulemakings can be found in DOT reports. The timeline for future rulemaking is pending on implementing Executive Orders. Enforcing the Regulatory Reform Agenda aims to allevia

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Overview of FDA Office of Regulatory Affairs (ORA) and Office of Regulatory Science (ORS)

This information provides insights into the organizational structure and functions of the FDA Office of Regulatory Affairs (ORA) and the Office of Regulatory Science (ORS). It includes organizational charts, details about ORA laboratory locations, and the local structure of an ORA laboratory. Additi

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Updates to ISO/IEC Directives Part 1 and IEC Supplement in 2023

In 2023, significant changes have been introduced to the ISO/IEC Directives Part 1 and IEC Supplement, impacting committee operations. These changes include the establishment of a joint SEG on Metaverse, clarification of participation criteria for P-Members, and guidelines for changing project leade

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Mitigation of Regulatory Capture in Economic Regulation

Regulation aims to correct market failures for societal welfare, but regulatory capture by interest groups can hinder regulatory actions. This work discusses economic theories on regulatory capture, forms of capture, and strategies to mitigate risks, emphasizing the public interest theory as a promo

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Overview of Energy Policy and Compliance with EU Directives in Georgia

Ministry of Energy in Georgia focuses on strategic directions for energy policy in alignment with EU directives. The Energy Strategy, Covenant of Mayors, and National Energy Efficiency Action Plan are key initiatives promoting energy efficiency and renewable energy. Projects include consultancy on s

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Challenges and Considerations in Regulatory Cooperation and Competition

Protecting consumers and investors through effective regulation of accounting and corporate financial reporting is crucial. Regulatory cooperation offers benefits like simplifying the regulatory environment and enforcing best practices. However, regulatory competition can uncover limits and the adva

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Importance of Advance Medical Directives in Estate Planning

Understand the significance of advance medical directives in estate planning to ensure your healthcare wishes are respected. Learn how these legal documents, containing a healthcare power of attorney and living will, benefit both you and your loved ones. Find out where to obtain an advance medical d

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Understanding Advanced Directives and Power of Attorney

Advanced directives and power of attorney are legal documents that allow individuals to plan for their medical care in case they become incapacitated. Advanced directives include instructions about life-sustaining treatments in terminal or irreversible conditions, while power of attorney delegates d

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Interdisciplinary Perspectives on End-of-Life Care

Exploring end-of-life care through an interdisciplinary lens, this presentation delves into social work, physical therapy, pharmaceutical aspects, and recommended interventions. Delicate considerations, diverse viewpoints, and evolving challenges in end-of-life decisions are examined, along with the

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Understanding Health Care Decision Laws in Tennessee

The Health Care Decision Act of 2004 in Tennessee ensures patients have the right to make their own health care decisions and promotes advance directives. Federal laws like the Patient Self-Determination Act of 1991 require health care facilities to provide statements of rights on decision-making an

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Understanding Advance Directives and End-of-Life Healthcare Planning

Advance directives are legal documents that enable individuals to express their medical care preferences for future situations when they may not be able to do so. Key components of advance directives include a durable power of attorney for healthcare, who to appoint, creating a living will, and unde

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Combating Ageism in Insurance: Equality Law Perspectives

Combating ageism attitudes in health and age-related insurance through equality law perspectives is crucial in ensuring fair treatment for all individuals. Directives such as Council Directive 2004/113/EC and Equal Status Act 2000 aim to prevent discrimination based on various factors including age,

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Parallel Programming Directives and Concepts

Learn about parallel programming directives like Diretiva.parallel and #pragma omp.parallel, which allow code to be executed by multiple threads simultaneously. Explore concepts such as defining parallel regions, setting the number of threads, and utilizing OpenMP directives for parallel for loops.

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Understanding the Victorian Regulatory Change Measurement (RCM)

The Victorian Regulatory Change Measurement (RCM) methodology introduced in June 2010 aims to measure reductions in regulatory burden through different categories such as administrative costs, substantive compliance costs, delay costs, and more. The RCM formula helps in calculating the total regulat

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Introduction to OpenMP: A Parallel Programming API

OpenMP, an API for multi-threaded, shared memory parallelism, is supported by compilers like C/C++ and Fortran. It consists of compiler directives, runtime library resources, and environment variables. The history spans various specification versions, with features like tasks, SIMD, and memory model

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National and EU Regulatory Frameworks for Training and Innovation Opportunities

Start/end date for WP5.1 initiative is M7-M24, led by CONFAGRI.PT and partners. The project aims to prepare the roll-out of deliverables at national and regional levels, focusing on regulatory frameworks, sustainability plan, and stakeholder engagement. Various organizations contribute to provide EU

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Michigan Physician Orders for Scope of Treatment (MI-POST) Training Overview

Explore the training objectives, target audience, and key information on Michigan Physician Orders for Scope of Treatment (MI-POST), including advance care planning, understanding advance directives, and types of Michigan advance directives. Learn about communication of care wishes, troubleshooting

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European Union Regulations and Directives on Marine Litter and Waste Management

Marine litter poses a significant threat to the marine environment, prompting the adoption of various international, regional, and national instruments to address the issue. Key directives such as the Marine Strategy Framework Directive and Waste Framework Directive set out measures to achieve good

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Challenges and Solutions in Implementing Regulatory Impact Assessment in India

This article explores the adoption of Regulatory Impact Assessment (RIA) in India, discussing the political economy challenges and strategies to overcome roadblocks. It outlines the working definition of RIA, addresses potential opposition from politicians and bureaucrats, and suggests ways to gener

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Understanding Good Regulatory Practice in Trade Governance

Good Regulatory Practice (GRP) is a key aspect of regulatory policy that focuses on improving the quality and cost-effectiveness of domestic regulations. It involves internationally recognized processes such as impact assessment, regulatory transparency, participation, and accountability. The import

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Regulatory Compliance for PU Products in Food and Drinking Water Contact

This document outlines the regulatory requirements for polyurethane (PU) products used in food and drinking water contact, including guidelines for monomers, additives, and substances allowed, as well as compliance procedures for both food and drinking water directives. It also details service activ

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Comprehensive Analysis of Rulemaking in Regulatory Governance

The executive review delves into regulatory materials from various chapters, highlighting both successes and failures within the regulatory landscape. It explores the tension in rulemaking, public perception of risk, and the role of non-agency regulation in tort and compensation law. The discussion

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Grant Management Directives and Personnel Name Changes Overview

Exploring Grant Management Directive 3 which details the process for Personnel Name Changes and Project Modifications. It emphasizes the importance of notifying the grant manager in writing within a specific timeline and outlines the steps involved in initiating a Personnel Name Change. Compliance w

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Essential Estate Planning and Advance Directives Guidance

Gain valuable insights into advance directives and estate planning essentials offered by the Law Office of Pamela G. Martini, PLLC. Learn about health care and financial decision makers, document accessibility, necessary steps, and key considerations. Understand Florida laws regarding health care pr

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Analysis of Medical Device Certificates Issued in Europe

This data analysis presents information on the distribution of valid certificates, new certificates issued, and distribution between different directives and conformity assessment modules for medical devices in Europe. The data covers the years 2010, 2012, and 2013, providing insights into the numbe

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