The contributions on data protection in the Land Registry questionnaire, discussing how different countries balance data protection with transparency in their online land registration systems.

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Explore the latest data and graphs from the ANZDATA Registry's 46th Annual Report regarding paediatric patients with kidney failure requiring replacement therapy. Discover trends in incidence, prevalence, educational participation, body mass index, hemoglobin levels, use of erythropoietic agents, fe

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Explore the various components of the Health Worker Information System, from registering new health workers to updating their credentials and querying for information. This system involves OpenInfoMan, Facility Registry, DHIS2, PR Data Store, Professional Councils, MOHSW HR System, and OpenHIE Provi

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Explore the purpose and requirements of the OBRA Nurse Aide Registry, including the importance of fulfilling nursing-related duties, regulations governing the registry, and what the registry is not responsible for. Learn about completing and submitting the Nursing Assistant Registry Inquiry Form and

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The UK Renal Registry's 24th Annual Report provides comprehensive data and insights on renal health in the UK up to 31st December 2020. The report covers various aspects such as patient outcomes, treatment trends, and demographic characteristics, highlighting the challenges and progress in the manag

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Clinical registries play a crucial role in tracking real-world data and outcomes for various medical conditions. They are observational databases that collect data systematically for specific purposes. Distinct from clinical trials, registries provide insights into broader patient populations and re

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The document provides an overview of the master facility lists (MFLs) in Nigeria, focusing on the rollout of the Health Facility Registry (HFR) for states and local government areas. It discusses the elements of functional MFLs, the process of facility listing, HFR development, governance plans for

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The process of establishing a Master Facility List (MFL) in a Health Facility Registry involves integrating data collection into routine facility visits, identifying data components, validating lists, and merging information at state level. Key elements include signature domain data (facility ID, ge

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The Civil Identity Registry System in Papua New Guinea, established by an Act of Parliament in 1963 and amended in 2014, plays a crucial role in maintaining records for births, marriages, adoptions, divorces, and deaths. The system faces challenges with data sharing due to legislation constraints. T

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Nigerian Internet Registration Association (NIRA) manages Nigeria's country code top-level domain (.ng). NIRA was established in 2005 after the delegation of .ng to Nigeria. The .ng Registry design includes a 3R model, public WHOIS server, EPP interface, and security measures like redundant site net

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The UK Renal Registry's 23rd Annual Report provides detailed data on patients starting renal replacement therapy (RRT) up to December 31, 2019. The report includes figures illustrating dialysis use, RRT incidence rates by country and age group, transplant status analysis, and RRT modality outcomes f

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European legislation provides definitions of key concepts for the land registry scope. Regulations and Directives focus on credit agreements, jurisdiction, succession, insolvency, matrimonial property regimes, and registered partnerships. These definitions are formal and abstract, aiming to encompas

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Managing the rollout of a Health Facility Registry/Master Facility List for states and local government areas in Nigeria involves creating, updating, deleting, and tracking facility records. The process includes data entry, approval procedures, and tracking request statuses for visibility to the pub

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Data submission in cancer registry systems serves the purpose of contributing to a larger pool of information for monitoring cancer trends, determining patterns, guiding program planning, and assisting public health professionals. Organizations like the State Central Cancer Registries and national p

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The National Joint Registry provides comprehensive data and reports on hip and knee replacements since 2003, including ankle, shoulder, and elbow replacements. The 9th Annual Report up to December 2011 highlighted key statistics, such as total activity, patient consent rates, and clinical activity d

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Hip fractures in Sweden pose significant challenges due to increased mortality rates. A retrospective cohort study analyzed data from the Swedish PeriOperative Registry to identify factors influencing patient outcomes post-surgery, highlighting the importance of various perioperative variables on lo

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Updates and discussions from the EGI Marketplace Service Registry Meeting on sustainable business models, requirements, and recent project developments. Focus on designing the EGI Service Registry and Marketplace with diverse input and limited budget considerations.

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The Service Registry and Marketplace aims to provide an open and comprehensive platform for researchers to register and share resources across academic and commercial providers. It offers fine-grain access control, supports internal and external resource sharing, and engages a wide network of users

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The UK Renal Registry 23rd Annual Report Data for the year 2019 provides detailed insights into the pathways, modalities, and primary renal diseases affecting children and young people (<16 years old) requiring renal replacement therapy (RRT). The report includes figures on RRT modalities, compariso

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Experience the journey of establishing a national registry for spinal pathologies in Belgium, led by Johan G. Van Lerbeirghe. Explore the goals, history, and the significance of choosing Spine Tango as the registry platform. Witness the challenges, partnerships, and milestones in the Belgian Pilot p

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This registry, established in 2014, aims to promote awareness, ensure accountability, and evaluate policy reforms related to prosecutorial misconduct, highlighting the prevalence of wrongful convictions due to such misconduct. It serves as a mechanism to document cases of misconduct, provide data fo

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Explore the justification, infrastructure, and progress of the National Childhood Cancer Registry (NCCR), focusing on the top causes of childhood cancer deaths, new diagnoses in 2017, and the importance of central cancer registry data. Discover the NCCR's coverage and efforts in residential history

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The UK Renal Registry 24th Annual Report Data provides comprehensive insights into renal health and patient outcomes up to 31/12/2020. The report covers a wide range of data including treatment trends, patient demographics, transplant outcomes, and more. It serves as a valuable resource for healthca

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Amid macroeconomic challenges and a changing financial sector landscape, Liberia faced prior obstacles including a lack of legal framework and centralized registry for collateral. The Collateral Registry Implementation aimed to address these issues, enhancing the country's secured transaction regime

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The Vascular Ultrasound Registry Pilot Project, led by Dr. David Dawson and Dr. Gregory L. Moneta, aims to enhance research, education, and quality in vascular ultrasound. This initiative involves a formal collaboration between SVS PSO, SVU, and M2S/Medstreaming to integrate images and data into cli

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Describing and sharing scientific datasets can be challenging due to the complexity and implicit assumptions involved. The Data Type Registry (DTR) addresses this issue by providing a systematic approach to define and record data assumptions, making data more accessible and reusable. Through DTR, da

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The Ely Diocesan Registry plays a crucial role in handling legal matters for Churchwardens. It is responsible for processing petitions, issuing documentation, providing legal advice, and maintaining various records related to the Church of England. Through its operations, the Registry supports clerg

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Explore the latest data from the UK Renal Registry's 24th Annual Report up to 31/12/2020 through a series of informative images. Gain valuable insights into renal health trends and statistics in the UK.

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The International Thoracic Organ Transplant Registry of the International Society for Heart and Lung Transplantation published its Thirty-Sixth Annual Report in October 2019. The report includes data from major contributors to the registry, acknowledgments to those involved, the TTX Registry Steerin

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The Kentucky Cancer Registry addresses the impact of COVID-19 on cancer patients, highlighting increased risks, altered treatment plans, and the importance of adjusting therapies to reduce infection rates. The registry emphasizes the higher incidence of COVID-19 in cancer patients compared to the ge

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The UK Renal Registry's 24th Annual Report provides comprehensive data and analysis up to 31st December 2020, covering various aspects related to renal health in the UK. The report highlights key findings, trends, and outcomes in renal care, including information on treatments, patient demographics,

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The UK Renal Registry's 23rd Annual Report provides comprehensive data on the pathways followed by adult patients to be included in the UK 2019 prevalent ICHD population. The report includes figures on percentage of patients with URR >65%, median URR achieved, changes in URR by sex between 2009 and

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Develop and maintain the C3S Data Rescue Portal with a global registry for data rescue activities, focusing on registering metadata, providing searchable inventories, and supporting DARE activities. The project aims to update inventories, facilitate data uploads, and offer user support and technical

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The UK Renal Registry's 22nd Annual Report presents detailed data on pathways and modalities for pediatric patients with chronic kidney disease. Figures from the report highlight the start of renal replacement therapy (RRT), prevalent RRT modalities, primary renal diseases, z-scores for height, and

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The UK Renal Registry's 25th Annual Report Data up to 31/12/2021 provides valuable insights into renal health statistics and trends in the UK. The report covers various aspects of renal care, including patient outcomes, treatment modalities, and demographic information. It serves as a comprehensive

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The UK Renal Registry's 25th Annual Report provides comprehensive data and insights on renal health up to 31st December 2021. The report covers various aspects such as prevalence, incidence, treatment modalities, and outcomes related to renal diseases in the UK population. It offers valuable informa

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Belgium's national cancer registry, established in 2004, covers a population of 11 million with data available since 2004. The registry includes specific legislation and authorization for data use, ensuring quality data collection and longitudinal follow-up. Various data sources feed into the regist

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The UK Renal Registry's 22nd Annual Report Data to 31/12/2018 provides detailed insights into various aspects of renal replacement therapy (RRT) initiation, incidence rates, primary renal diseases, RRT modalities, and more. The report includes figures illustrating RRT initiation patterns, adult RRT

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The UK Renal Registry's 24th Annual Report Data provides comprehensive insights and statistics on renal health up to 31st December 2020. The report covers a wide range of topics related to kidney diseases, treatment trends, patient demographics, and outcomes, offering valuable information for health

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The Corporate Registers Forum (CRF) is an international organization dedicated to fostering collaboration among administrators of corporate registers worldwide. Established in 2006, the CRF aims to facilitate the exchange of information, address registration challenges, and promote efficient registr

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