Regulatory affairs - PowerPoint PPT Presentation


Department of Home Affairs Quarterly Performance Presentation 2022/2023

Presentation to the Portfolio Committee on Home Affairs featuring the 3rd and 4th quarterly performance reports and budget versus expenditure reports of the Department of Home Affairs for 2022/2023. The report outlines the vision, mission, and value statement of the department, along with its mandat

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Department of Home Affairs 2023/24 Annual Performance Plan Presentation

Presentation of the 2023/24 2nd quarterly performance report and budget versus expenditure report to the Portfolio Committee on Home Affairs. The content includes the vision, mission, and value statement of the Department of Home Affairs, its mandate, outcomes, overall performance for the quarter, p

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Gene Therapy and Genome Editing Technology

This article provides insights into the status, regulatory considerations, and delivery methods of gene therapy and genome editing technologies. It discusses approved gene therapies in the US, human genome editing in clinical applications, and the regulatory authority of the FDA over gene therapy. T

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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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International Perspective on SMEs Regulatory Framework with Iberoamerican Network of Guarantees

The regulatory framework of SMEs, particularly within the Iberoamerican Network of Guarantees (REGAR), showcases the establishment and operations of guarantee schemes in various countries such as Spain, Mexico, Portugal, and others. The warranty industry has witnessed global expansion with diverse m

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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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Environmental Protection Strategies and Regulatory Framework Summary

Explore the comprehensive planning drivers, regulatory challenges, and implementation pathways in the environmental protection domain. Key elements include the strategic roadmap, funding priorities, regulatory analysis, and collaborative permitting strategies. Navigate the complexities of environmen

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Overview of Guam Regulatory Aquifer Mapping and Groundwater Protection

Guam's Regulatory Aquifer Mapping includes conflicting maps from USEPA, the Northern Guam Lens Study, and Groundwater Protection Zones, impacting land use regulations and water quality standards. Issues arise from inconsistencies in regulatory tools and language errors within the protection zones. Z

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the Impact of Regulatory Changes on Cargo Pricing Technology

In today's rapidly evolving global trade landscape, the logistics industry is no stranger to constant regulatory changes. These changes not only affect operational procedures but also have a significant impact on cargo pricing technology. As revenue technology services continue to innovate to meet t

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IAS Current Affairs

Stay ahead in your IAS preparation with IASexam.com, the ultimate destination for IAS current affairs. Our platform is meticulously designed to provide aspirants with the most up-to-date, relevant, and comprehensive coverage of current affairs crucial for the IAS examination. At IASexam.com, we unde

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Medical Device & Diagnostics Regulatory, Compliance, Post-Market Surveillance

In the heart of Dusseldorf, Germany, the MarketsandMarkets European Medical Device & Diagnostics Regulatory, Compliance, Post-Market Surveillance and Vigilance Conference is set to unfold on the 14th and 15th of October 2024.\n\nRegister Now @ \/\/events.marketsandmarkets.com\/european-medical-devic

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Task Force Report on Regulatory Fitness for Automated Driving Systems

The co-chairs of the Task Force on Regulatory Fitness for Automated Driving Systems presented an informal document at the 19th meeting of GRVA, outlining the context, purpose, and status of regulations related to automated vehicles. The report focuses on the need for a regulatory environment for aut

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Understanding Stewardship in Student Affairs: Principles and Values

Stewardship in Student Affairs involves effective management and safeguarding of resources like time, money, and people. This session delves into the principles of stewardship, rooted in priorities and values, emphasizing transparency, accountability, and adaptability. It also highlights the Divisio

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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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Understanding the BVIs FinTech Regulatory Sandbox

The BVIs FinTech Regulatory Sandbox aims to promote efficiencies, leverage technology for innovative financial solutions, provide regulatory clarity, and develop targeted responses. Eligible persons include startups proposing new financial services, innovative technologies for licensable services, a

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COVID-19 Vaccines Regulatory Status Update - SAHPRA Review Details

Update on COVID-19 vaccine regulatory status as of January 25, 2021, provided by Dr. B. Semete-Makokotlela, SAHPRA CEO. The update includes information on vaccine applications submitted to SAHPRA, regulatory reviews conducted, and Section 21 applications for vaccines like Janssen, AstraZeneca, and C

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Regulatory Advisory Panel Meeting - October 14, 2020

The Regulatory Advisory Panel meeting held on October 14, 2020, at 3:30 p.m. covered roll call details of attendees from various organizations and agencies. The meeting focused on key members and workgroup organizations pertaining to health care, hospice, and regulatory affairs. Attendees were urged

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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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Fuel Pricing Mechanisms and Regulatory Framework Presentation

This presentation to the Portfolio Committee on Mineral Resources and Energy delves into the Basic Fuel Price (BFP) for liquid fuels, covering global fuel pricing forms, policy positions, key pricing mechanisms, regulatory mandates, and the intricate structure behind fuel prices. It explains how the

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Overview of Pharmacy Law and Regulatory Affairs

This comprehensive guide covers the definitions, licensing requirements, rules and regulations, drug classifications, establishment classifications, Ministry of Health licensing requirements, and general application and licensing requirements in the field of pharmacy law and regulatory affairs. It i

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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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Targeted Learning Framework for Causal Effect Estimation Using Real World Data

Hana Lee, Ph.D., presents a webinar on the Targeted Learning Framework for Causal Effect Estimation using Real World Data (TMLE). The project aims to help the FDA develop a structured approach to incorporating real-world data into regulatory decision-making. TMLE offers a systematic roadmap aligned

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Overview of Medical Devices and Regulatory Compliance

Introduction to medical devices, including definitions, classifications, and major groups of instruments. Learn about the technical and general definitions, the benefits of medical devices for patients, and the expertise required in regulatory affairs and quality management systems.

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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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Ethical Conduct of Research in Veterans Affairs: Compliance and Oversight

The Department of Veterans Affairs upholds ethical standards in research involving animals, focusing on minimizing pain and distress while ensuring scientific necessity. Compliance with various regulatory requirements, including USDA, PHS, and AAALAC, is essential to demonstrate ethical responsibili

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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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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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MEHA Body Art Enforcement Presentation Summary

In the "MEHA Body Art Enforcement Presentation of 3-16-2016," the implementation by Deborah Garcia focuses on reporting social media unlicensed body art facilities, cost estimates for tattoo equipment and supplies, legal affairs communications, and the agencies involved in Michigan's enforcement eff

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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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Faculty Governance at Saint Louis University School of Medicine

Explore the faculty governance structure at Saint Louis University School of Medicine, including departmental meetings, committees, Faculty Assembly, Faculty Affairs Committee, and the University Faculty Senate. Learn about the roles of various elected positions, such as the Executive Committee and

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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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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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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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Roundtable Discussion on The 19th National Congress of CPC Moderator's Bio

Miaoqiang is a Master of International Affairs, President of Research and Career Development Network for Law and International Affairs. Dr. Flora Sapio, a Board Member of FLIA, is internationally renowned for her analyses in China studies. Larry Backer, Professor of Law & International Affairs, focu

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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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Affiliated Societies Meeting HKUST Students Union 2015-2016 Agenda

This document provides details about the Affiliated Societies Meeting of the HKUST Students Union for the year 2015-2016. It covers the agenda items such as introduction, report of orientation affairs, Green O Camp project, important dates for O Camp documents submission, and a Q&A session. It also

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RAC Exam I Test Questions

The RAC Exam I Test Questions cover various aspects of regulatory affairs and compliance in the pharmaceutical industry. The questions touch on topics such as GMP, FDA regulations, product approvals, and legal requirements. Test your knowledge with these 100 questions to enhance your understanding o

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Presidential National Security Powers: Summary of Basic Principles

In Zivotofsky II, the Supreme Court recognized the President's exclusive implied powers despite acknowledging the role of Congress in lawmaking. While the President engages in foreign affairs activities, no general plenary and exclusive foreign affairs power is explicitly vested in the Constitution.

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