Pet registry – Codogfederation http://codogfederation.org/ Sun, 28 Nov 2021 03:14:48 +0000 en-US hourly 1 https://wordpress.org/?v=5.8 https://codogfederation.org/wp-content/uploads/2021/10/icon-71-120x120.png Pet registry – Codogfederation http://codogfederation.org/ 32 32 Registry Dethrones School at the 31st ISL Sports Meeting – :::… The Tide News Online :::… https://codogfederation.org/registry-dethrones-school-at-the-31st-isl-sports-meeting-the-tide-news-online/ Fri, 26 Nov 2021 02:48:14 +0000 https://codogfederation.org/registry-dethrones-school-at-the-31st-isl-sports-meeting-the-tide-news-online/ The Registry (Red House) filed the Scholarship (White House) to win the 31st International School of Inter-House Athletics Competition, University of Lagos (ISL), held at the International School Sports Ground, University from Lagos.Registry won 14 gold, seven silver and four bronze, while Congregation (Purple House) finished second with nine gold, seven silver and 10 bronze.The […]]]>

The Registry (Red House) filed the Scholarship (White House) to win the 31st International School of Inter-House Athletics Competition, University of Lagos (ISL), held at the International School Sports Ground, University from Lagos.
Registry won 14 gold, seven silver and four bronze, while Congregation (Purple House) finished second with nine gold, seven silver and 10 bronze.
The Tidesports source reports that the Chancellery (Yellow House) finished third with seven gold, four silver and two bronze, while the Senate (Blue) placed fourth with four gold, 15 of silver and eight of bronze.
Bursary (White House) occupied the fifth position with four gold, five silver and 11 bronze, however, the defending champion, School (Green House), came sixth in the standings after winning three medals of ‘gold, three of silver and six of bronze.
In the last run, the Senate came out on top with 93 points, the stock market was second with 89 points, while the school had 88 points to get the third position, the record fourth with 83 points, the congregation fifth with 78 points and the sixth chancellery with 76 points.
Mohammed Femisola was voted best athlete after winning four gold medals in the 800 meters, 1500 meters, 400 meters and 4 × 100 meters.
Speaking at the event, the school’s acting principal, KO Amusan, said the competition was part of the school’s extracurricular activities that encourage healthy lifestyles and expose students’ hidden talents.
“We are here to celebrate our 31st inter-house sports competition. It is a special event because our school has just celebrated its 40th anniversary and it is our 40th edition of Founders’ Day. This year’s competition is very unique as we are using our own pitch for the first time compared to the University of Lagos Sports Center, which we have used in the past.
“When we talk about a school setting, school isn’t just about academics because they say all work and no play makes Jack a boring boy. Inter-house sports competition is very important because it allows for healthy competitions between students and even staff. The health benefits are numerous, ”he said.
Also speaking at the event, the Occasion Chairman and Group Managing Director of Vita Foam Nigeria Plc, Mr. Taiwo Ayodele Adeniyi, who was represented by Mr. Owabamidele Sola, said the event was a celebration of youth, adding that it occupied a very important place. in the countryside.
“For a country to grow, we must encourage it to show all the potential that God has placed in it. The competition is also an opportunity for students to develop their talents outside academics. And legal persons have a duty to support grassroots sport and all that is good.
This is why Vita Foam is known, because we are a brand that supports talent when we see where talent is developing and we nurture it, ”he said.


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Patient Registry Software Market to Advance Global Unexpected Growth and Market Opportunities 2021-2030 | Taiwan News https://codogfederation.org/patient-registry-software-market-to-advance-global-unexpected-growth-and-market-opportunities-2021-2030-taiwan-news/ Mon, 22 Nov 2021 06:42:36 +0000 https://codogfederation.org/patient-registry-software-market-to-advance-global-unexpected-growth-and-market-opportunities-2021-2030-taiwan-news/ MarketResearch.biz released the report titled, Global Patient Registry Software Market Growth Trends, Analysis, Drivers and Forecasts up to 20%30. The report offers in-depth information of the major players operating in the global Patient Registry Software market, which further includes their financials, aside from strategies, acquisitions & mergers, and market footprint. This report also offers in-depth […]]]>

MarketResearch.biz released the report titled, Global Patient Registry Software Market Growth Trends, Analysis, Drivers and Forecasts up to 20%30.

The report offers in-depth information of the major players operating in the global Patient Registry Software market, which further includes their financials, aside from strategies, acquisitions & mergers, and market footprint. This report also offers in-depth insights, revenue details of Patient Registry Software market, and other significant insights about the global Patient Registry Software market and various trends, drivers, restraints, opportunities in the Patient Registry Software market. patient registry software and threats, until 2030.

This Patient Registry Software market research report also includes PEST analysis, PORTER’s five forces analysis in Patient Registry Software Market


To assimilate the full report via table of contents, figures and tables, request a sample copy @ @ https://marketresearch.biz/report/patient-registry-software-market/request-sample

The report contains a full analysis:

• Current trends in the patient registry software market

• Drivers, Constraints and Opportunities of the Patient Registry Software Market

• Segmentation of the patient registry software market

• Competition from domestic producers and imports

• Geographical analysis of the production of the patient registry software

• Key strategic players

Leading companies operating in the area of ​​Patient Registry Software market are:

  • Global Vision Technologies, Inc.
  • Quintiles, Inc.
  • Dacima Software Inc.
  • Globus Medical, Inc.
  • PatientCrossroads, Inc.
  • eClinical Solutions LLC
  • Mckesson Company
  • Liaison Technologies, Inc.
  • ImageTrend, Inc.
  • FIGMD, Inc

which further covers the company overview, product portfolio, financial presentation, key developments and SWOT analysis on the Patient Registry Software Market scenario.

For any question or customization related to the same, inquire here @ https://marketresearch.biz/report/patient-registry-software-market/#inquiry

The Global Patient Registry Software Market report has been segmented as follows:

Segmentation by software type:

  • Integrated software
  • Standalone software

Segmentation by delivery method:

  • On the spot
  • Cloud / web based

Segmentation by functionality:

  • Population health management
  • Exchange of health information
  • Point of service
  • Others (evaluation of product results, medical research and clinical studies, etc.)

Segmentation by end user:

  • Hospitals
  • Government organization
  • Research centers
  • Pharmaceutical, biotechnology and medical device companies

Segmentation by region:

  • North America
  • Europe
  • Asia Pacific
  • Latin America
  • Middle East and Africa

COVID-19 impact assessment:

– The overall state of the Patient Registry Software market has been carefully assessed with pandemic outrage and accurate predictions have also been made to assist with futuristic growth projections.

– Changes in the parameters of supply chain dynamics have been discussed in this study report.

– The long and short term consequences of the market growth accumulated by the evolution of the affected company, with a major pandemic.

Find out what is the impact of COVID 19 on the Patient Registry Software Market and how the market will grow over the next period 2021-2030.

Download now (short and long term) the COVID 19 impact analysis [PDF] Patient Registry Software Market Report >>https://marketresearch.biz/report/patient-registry-software-market/ covid-19-impact

Global Patient Registry Software Market Segmentation by Region: Covers market share and forecast, as well as year-over-year growth, 2021-2031 (USD Million).

  1. North America
  2. Asia Pacific
  3. Europe
  4. Latin America
  5. The Middle East and Africa

Highlights of the Patient Registry Software Market Report:

Sales volume via manufacturers: This section of the report provides information on sales, manufacturing and capacity of major producers, value through producers, expansion plans, mergers and acquisitions and commodities, market entry dates , distribution and market regions.

Market size by type: This phase focuses on product type segments, mentioning market proportion of manufacturing value, value and proportion of manufacturing market by product type.

Market Volume by Application: In addition to an overview of the global postal securities market via the app, it provides a review of the contribution to the global postal securities market via the app.

Manufacturing by region: This section provides information about the manufacturing value increase price, the manufacturing increase price, import and export, and the major suppliers in each local market.

Company version reports: Almost all of the major vendors in the global postal securities market professionally report on this phase. The analysts provided information on their most recent trends in the global job titles market, commodities, sales, manufacturing, businesses and agencies.

Industry Forecast Through Manufacturing: This phase includes manufacturing and manufacturing value forecasts for the global postal securities market as well as major local markets.

For more details or any customization of the report, please connect with our sales team @ inquiry@marketresearch.biz

Research objectives:

1. To study and analyze the global Patient Registry Software market size by key areas / countries, product type and application, historical data.

2. Understand the structure of Patient Registry Software market by identifying its various subsegments.

3. Focuses on the major global players in Patient Registry Software, to define, describe and analyze the value, market share and development plans over the next few years.

4. To analyze the Patient Registry Software with respect to individual growth trends, future prospects, and their contribution to the total market.

5. Share detailed information on key factors influencing market maturity.

6. To project the size of Patient Registry Software submarkets, with respect to key regions (along with their respective key countries).

7. Investigate aggressive market developments such as market expansions, agreements, new product launches and acquisitions.

8. Develop a strategic profile of key players and thoroughly review their growth plans.

To buy Full premium research report activated with respective tables and figures on https://marketresearch.biz/purchase-report/?report_id=7579

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3. Animal health market status, key trends and prospective 2021-2030

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What happened to the “Do Not Call Register?” “- WWLP https://codogfederation.org/what-happened-to-the-do-not-call-register-wwlp/ Sun, 21 Nov 2021 15:19:28 +0000 https://codogfederation.org/what-happened-to-the-do-not-call-register-wwlp/ Single-family home sales in Massachusetts fell dramatically in October Video / 2 days ago Video Man arrested after unrest on Longhill Street in Springfield Video / 2 days ago Video 230 illegally detained firearms seized by Springfield police this year Video / 2 days ago Video “If you don’t obey the sign, you can expect […]]]>

Single-family home sales in Massachusetts fell dramatically in October

Video /

Man arrested after unrest on Longhill Street in Springfield

Video /

230 illegally detained firearms seized by Springfield police this year

Video /

“If you don’t obey the sign, you can expect to be fined,” said Captain Dave Martin of the Springfield Police Traffic Bureau.

Video /

“Be careful, slow down, don’t think this can’t affect you,” Springfield Police Commissioner Cheryl Clapprood

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St. Mary’s Schools in Westfield Switch to Distance Learning Amid Rising COVID-19 Cases in City

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Rising costs of hospital care

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Thursday Night Football: Patriots vs. Falcons

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Hampden County drug money seized attributed to nonprofits

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COVID-19 booster shots approved for all Massachusetts residents over 18

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ValleyBike Share will remain available during the winter months

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3-Day Detour: Elm Street and Franklin Street Traffic Lights Out of Westfield

Video /


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Euro Roundup: EMA issues directive on conducting registry-based studies https://codogfederation.org/euro-roundup-ema-issues-directive-on-conducting-registry-based-studies/ https://codogfederation.org/euro-roundup-ema-issues-directive-on-conducting-registry-based-studies/#respond Thu, 28 Oct 2021 17:39:31 +0000 https://codogfederation.org/euro-roundup-ema-issues-directive-on-conducting-registry-based-studies/ The European Medicines Agency (EMA) has published recommendations on the main methodological aspects specific to the conduct of registry-based studies by marketing authorization holders and applicants. The EMA, as part of its Patient Registries Initiative and Inter-Committee Registries Working Group, explored ways to improve the use of patient registries to support regulatory decision-making. The project […]]]>

The European Medicines Agency (EMA) has published recommendations on the main methodological aspects specific to the conduct of registry-based studies by marketing authorization holders and applicants.

The EMA, as part of its Patient Registries Initiative and Inter-Committee Registries Working Group, explored ways to improve the use of patient registries to support regulatory decision-making. The project resulted in a series of workshops which generated recommendations and later a discussion paper. Today, the EMA has brought together information and recommendations from other groups in the European Union and overseas into a directive on registry-based studies.

The guideline distinguishes between registries and registry-based studies, explaining that in the latter a specific research question is examined “using the data collection infrastructure or the patient population of one or more registries. of patients ”. The length of follow-up, patient recruitment and data collection are all dictated by the research question.

Elsewhere in the directive, the EMA explains how marketing authorization holders and applicants can use the results of registry-based studies. The acceptability of the evidence from the studies depends on the product, the registry and the study, leading the EMA to advise drug developers to consult it promptly or to consult a competent national authority.

The EMA identifies a range of potential uses for the results of registry-based studies. Pre-authorization, the agency expects preclinical studies and clinical trials to form the core of the evidence for a drug. Yet registry-based studies can play a role, for example by providing evidence of how a disease is treated in the real world or by contextualizing the results of uncontrolled clinical trials. When using evidence pre-approval, the EMA recommends discussing the acceptability of the proposed approach with regulators, health technology assessment bodies and payers.

A different set of use cases apply once a product is on the market. “Patient registers can serve as the basis for recruitment and randomization for RCTs and non-interventional studies, post-authorization efficacy studies and post-authorization safety studies performed after marketing authorization. . They can allow patient records to be linked with other data sources such as biobank data, census data or demographic data, ”says the directive.

The following section of the 35-page guideline describes how to plan a registry-based study, design the protocol, select the patient population, and collect, analyze and report the data. These topics occupy approximately the first half of the document. The remainder of the guideline is devoted to legal issues, patient registry considerations and appendices such as a checklist for assessing the suitability of registries for registry-based studies.

EMA guideline

European Parliament votes for more transparent COVID-19 vaccination policies

The European Parliament has called for legislation to make the search, purchase and distribution of COVID-19 vaccines more transparent to help counter hesitation and misinformation about vaccines.

Many requests relate to current and future contracts between the Commission and manufacturers of COVID-19 vaccines. The resolution, which was adopted by 458 votes to 149, with 86 abstentions, calls on the Commission to publish without delay the unredacted versions of the purchasing contracts. Parliamentarians want the disclosures to cover the amount of public investment that has been spent on vaccine development, the prices and the number of doses sent to each country.

Other requests relate to clinical trial data. Politicians want the Commission to “ensure that contracted companies make available full clinical trial results and potential research protocols on a COVID-19 vaccine for evaluation, as soon as possible, by independent scientific experts,” beyond EMA experts ”. The request is for statistical analysis plans, clinical studies and reports.

Dolors Montserrat, chair of the petitions committee, made the demands as part of a campaign to tackle vaccine hesitancy. “The petitions show that some citizens are reluctant to get vaccinated. This is why we need to be transparent about how COVID-19 vaccines are developed, procured and distributed. For the strategy to be successful, the public needs to receive more information, ”Montserrat said.

Press release, Resolution adopted

EMA answers questions about sending data to the EudraVigilance dictionary

The EMA answered dozens of frequently asked questions about electronic submission of investigational drug data to the EudraVigilance Extended Drug Dictionary (XEVMPD).

The document covers fundamental issues, such as the legal obligation to submit data, to more specific queries. More specific questions include: “In our clinical trial we are using a drug that is already authorized. However, it is being studied for a new indication not listed in the SPC. How should we submit such a product to XEVMPD? “

The EMA divided the beginning of the document into questions about submitting investigational drugs, drugs in development, and sponsor information. The rest of the text covers topics such as pharmaceutical information, printed product information, and chemical therapeutic anatomical code.

One question is whether promoters should submit placebos information to XEVMPD. The EMA said only information on the active ingredients of the investigational drug should be submitted, citing other documents to make its case.

EMA FAQ

MHRA calls on sponsors to use combined review route ahead of January change

The UK Medicines and Health Products Regulatory Agency (MHRA) has asked sponsors to start using its combined review channel for clinical trial applications. The combined review will become the way all filings will be processed from January, but the MHRA wants sponsors to use the lane before that date.

In an update to its guidelines on authorizing clinical trials, the MHRA said its combined review service, formerly known as Combined Ways of Working, will become the way all new trial applications Investigational Drug Clinics (CTIMP) are prepared, submitted and reviewed starting January 1. The combined review allows promoters to make a single filing and receive a single UK decision.

While the mandatory use of the track is still two months away, the MHRA is asking sponsors who “have new CTIMP applications planned in the weeks or months to come” to apply for a combined review.

Combined review requests “should be initiated and submitted using the new part of the Integrated Search Application System (IRAS) and not the standard part of IRAS,” the MHRA said. The regulatory requirements and fees are the same as for the old uncombined exam. However, the MHRA advises applicants to refer to the Health Research Authority’s website, rather than its guidelines, for information on the stages of submitting, processing, and reviewing the application.

MHRA Guidelines

Commission carries out unannounced antitrust inspections at animal health company

The European Commission carries out unannounced inspections of “a pharmaceutical company active in the field of animal health in Belgium”.

Officials launched the inspections over “concerns that the inspected company may have violated EU antitrust rules which prohibit abuse of dominance.” The Commission is working with the Belgian competition authority on inspections, which constitute a preliminary stage of investigation into suspected anti-competitive practices.

At this point, not much else is known for sure. The company has not been found guilty of anti-competitive behavior and the duration of the investigation will depend on a range of factors, such as the complexity of the case and the extent to which the company cooperates with the Commission.

Press release

Other news:

The EMA Committee for Medicinal Products for Human Use has decided that a booster dose of Moderna Spikevax’s COVID-19 vaccine can be considered in people 18 years of age and older. EMA opinion

© 2021 Society of Regulatory Affairs Professionals.


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Seno Medical Launches CONFIDENCE Registry Study for the Imagio® Breast Imaging System | Nation / World https://codogfederation.org/seno-medical-launches-confidence-registry-study-for-the-imagio-breast-imaging-system-nation-world/ https://codogfederation.org/seno-medical-launches-confidence-registry-study-for-the-imagio-breast-imaging-system-nation-world/#respond Thu, 21 Oct 2021 15:02:14 +0000 https://codogfederation.org/seno-medical-launches-confidence-registry-study-for-the-imagio-breast-imaging-system-nation-world/ San Antonio, TX, October 21, 2021 (GLOBE NEWSWIRE) – Texas-based Seno Medical Instruments, Inc. (Seno) has launched its CONFIDENCE registry to assess the effectiveness of opto-acoustic / ultrasound imaging (OA / US ) to diagnose breast abnormalities, including cancer, using its revolutionary Imagio® breast imaging system. About twelve sites will participate in the international registry, […]]]>

San Antonio, TX, October 21, 2021 (GLOBE NEWSWIRE) – Texas-based Seno Medical Instruments, Inc. (Seno) has launched its CONFIDENCE registry to assess the effectiveness of opto-acoustic / ultrasound imaging (OA / US ) to diagnose breast abnormalities, including cancer, using its revolutionary Imagio® breast imaging system. About twelve sites will participate in the international registry, with a target of more than 600 total patients participating throughout the study period, ending in 2024.

Several international sites in the Netherlands are currently recruiting for the study. The objective of the study is to obtain real post-market data on the use of the Imagio® system and to provide evidence of the general use and performance of the system in a real environment.

“We believe that, just like other hybrid imaging modalities such as PET / CT, the sum of optoacoustics and ultrasound provides greater sensitivity and specificity than either. individual imaging modalities, ”said Shaan Schaeffer, vice president of clinical operations at Seno.

The CONFIDENCE registry parameters to analyze include:

  • Specificity, negative likelihood ratio, sensitivity and positive likelihood ratio for the Imagio® system compared to other standard imaging modalities,
  • Use of the Imagio® system in comparison and in combination with other imaging modalities to influence the biopsy decision,
  • Quality of life assessment – Morbidity index test,
  • In malignant masses, evaluation of the roles of OA / US as a prognostic biomarker,
  • Characteristics of the lesions / masses of the lymph nodes for which the device is used.

Breast biopsy procedures caused by false positive diagnostic evaluations in the United States cost the healthcare system more than $ 2 billion per year.i Seno’s Imagio® technology could mitigate this with its non-invasive OA / US technology for helping physicians better differentiate malignant breast lesions in real time, helping providers characterize and differentiate masses that may or may not require more invasive diagnostic evaluation.

Seno CEO Tom Umbel commented: “This registry study will help us justify the effectiveness of the Imagio® system in a real world setting and the ability of OA / US to benefit physicians and patients. of the whole world.

The company’s OA / US technology combines laser optics and grayscale ultrasound to provide fused functional and anatomical breast imaging. Optoacoustic images provide a unique blood map in and around breast masses, while ultrasound provides a traditional anatomical image. By the appearance or absence of two characteristic indicators of cancer – angiogenesis and deoxygenation – Seno Medical has shown that the Imagio® OA / US breast imaging system will be a more effective tool to help radiologists confirm or exclude malignancy over traditional diagnostic imaging modalities – without exposing patients to ionizing radiation (x-rays) or potentially harmful contrast agents. In addition to the new imagery provided by the Imagio® system, Seno includes an artificial intelligence (AI) decision support tool (the SenoGram®) to help physicians interpret the new images which, along with training and certification, help radiologists make the transition from ultrasound alone to OA / US imaging.

The system is indicated for use by trained and qualified healthcare providers to assess palpable and non-palpable breast abnormalities in adult patients who are referred for diagnostic imaging breast exam following clinical presentation or breast cancer. ” other imaging tests such as a screening mammogram.

Seno Medical Instruments, Inc. is a San Antonio, Texas-based medical imaging company engaged in the development and commercialization of a novel cancer diagnostic modality: optoacoustic imaging. Approved by the US FDA in January 2021, Seno Medical’s Imagio® Breast Imaging System merges optoacoustic technology with ultrasound (OA / US) to generate functional and anatomical images of the breast in real time. To learn more about Seno Medical’s OA / US imaging technology and applications, visit www.SenoMedical.com.

###


i Vlahiotis A, Griffin B, Stavros AT, Margolis J. Analysis of use patterns and associated costs of breast imaging and diagnostic procedures after screening mammography. Clinicoeconomics Outcomes Res 2018; 10: 157-167.

Attachment

Tom Umbel Seno Medical 781-640-6828 tumbel@senomedical.com Tammy Garcia Seno Medical (210) 615-6501 tgarcia@senomedical.com

Copyright 2021 GlobeNewswire, Inc.


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Seno Medical launches the CONFIDENCE registry study for Imagio® https://codogfederation.org/seno-medical-launches-the-confidence-registry-study-for-imagio/ https://codogfederation.org/seno-medical-launches-the-confidence-registry-study-for-imagio/#respond Thu, 21 Oct 2021 15:00:00 +0000 https://codogfederation.org/seno-medical-launches-the-confidence-registry-study-for-imagio/ San Antonio, TX, October 21, 2021 (GLOBE NEWSWIRE) – Texas-based Seno Medical Instruments, Inc. (Seno) has launched its CONFIDENCE registry to assess the effectiveness of opto-acoustic / ultrasound imaging (OA / US ) to diagnose breast abnormalities including cancer using its revolutionary Imagio® Breast imaging system. About twelve sites will participate in the international registry, […]]]>

San Antonio, TX, October 21, 2021 (GLOBE NEWSWIRE) – Texas-based Seno Medical Instruments, Inc. (Seno) has launched its CONFIDENCE registry to assess the effectiveness of opto-acoustic / ultrasound imaging (OA / US ) to diagnose breast abnormalities including cancer using its revolutionary Imagio® Breast imaging system. About twelve sites will participate in the international registry, with a target of more than 600 total patients participating during the study period, ending in 2024.

Several international sites in the Netherlands are currently recruiting for the study. The aim of the study is to obtain real and post-market data on the use of the Imagio® system and provide evidence of general use and performance of the system in a real environment.

“We believe that, just like other hybrid imaging modalities such as PET / CT, the sum of optoacoustics and ultrasound provides greater sensitivity and specificity than either. individual imaging modalities, ”said Shaan Schaeffer, vice president of clinical operations at Seno.

The CONFIDENCE registry parameters to analyze include:

  • Specificity, negative likelihood ratio, sensitivity and positive likelihood ratio for the Imagio® System compared to other standard imaging modalities,
  • Using Imagio® System in relation to, and in combination with, other imaging modalities to influence the biopsy decision,
  • Quality of life assessment – Morbidity index test,
  • In malignant masses, evaluation of the roles of OA / US as a prognostic biomarker,
  • Characteristics of the lesions / masses of the lymph nodes for which the device is used.

Breast biopsy procedures caused by false positive diagnostic evaluations in the United States cost the health care system more than $ 2 billion annually.I Imagio de Seno® The technology could mitigate this with its non-invasive OA / US technology to help physicians better differentiate benign and malignant breast lesions in real time, helping providers characterize and differentiate masses that may or may not require more diagnostic evaluation. invasive.

Seno CEO Tom Umbel commented: “This registry study will help us justify the effectiveness of Imagio® The system in a real environment and the possibility for OA / US to benefit physicians and patients around the world.

The company’s OA / US technology combines laser optics and grayscale ultrasound to provide fused functional and anatomical breast imaging. Optoacoustic images provide a unique blood map in and around breast masses, while ultrasound provides a traditional anatomical image. By the appearance or absence of two characteristic indicators of cancer – angiogenesis and deoxygenation – Seno Medical has shown that Imagio® The OA / US Breast Imaging System will be a more effective tool in helping radiologists confirm or rule out malignancy compared to traditional diagnostic imaging modalities – without exposing patients to ionizing radiation (x-rays) or radiation. potentially harmful contrast agents. In addition to the new imagery provided by the Imagio® System, Seno includes an artificial intelligence (AI) decision support tool (the SenoGram®) to help physicians interpret the new images which, along with training and certification, help radiologists make the transition from ultrasound alone to OA / US imaging.

The system is indicated for use by trained and qualified healthcare providers to assess palpable and non-palpable breast abnormalities in adult patients who are referred for diagnostic imaging breast exam following clinical presentation or breast cancer. ” other imaging tests such as a screening mammogram.

Seno Medical Instruments, Inc. is a San Antonio, Texas-based medical imaging company engaged in the development and commercialization of a novel cancer diagnostic modality: optoacoustic imaging. Approved by the US FDA in January 2021, Imagio de Seno Medical® The breast imaging system merges opto-acoustic technology with ultrasound (OA / US) to generate functional and anatomical images of the breast in real time. To learn more about Seno Medical’s OA / US imaging technology and applications, visit www.SenoMedical.com.

###


I Vlahiotis A, Griffin B, Stavros AT, Margolis J. Analysis of use patterns and associated costs of breast imaging and diagnostic procedures after screening mammography. Clinico-economic results Res 2018; 10: 157-167.

  • Seno Medical launches the CONFIDENCE registry study for the Imagio® breast imaging system

        


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Man struck off sex offender register faces new sexual assault charges https://codogfederation.org/man-struck-off-sex-offender-register-faces-new-sexual-assault-charges/ Mon, 18 Oct 2021 07:00:00 +0000 https://codogfederation.org/man-struck-off-sex-offender-register-faces-new-sexual-assault-charges/ Victim helps police catch sexual assault suspect on new charges Jeanie Fulcher was only 7 years old when her cousin by marriage robbed her of her innocence. Derrick Crooms pleaded guilty to the crime in 1996. Today, 25 years later, he faces similar charges. When Fulcher heard of the 18 new charges of sexual assault […]]]>

After the withdrawal of Derrick Crooms from the Georgia Sex Offender Registry, he was again arrested on 18 charges related to To indecent assault, incest and rape.

“He took my innocence when I was seven,” said Jeanie Fulcher, now 34. “I don’t know if you can really get over this.”

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Fulcher said she decided to go public with her story to encourage other victims to speak to law enforcement.

Court records show that Crooms pleaded guilty in 1996 to sexual assault charges for what he did to Fulcher, his step cousin. A judge sentenced him to 20 years, but he only served four.

“It happened to me for a year before I had the courage to tell someone about it,” Fulcher said.

The U.S. Marshalls arrested the Covington man at a Stone Mountain home on Friday.

“In December 2020, the Child Exploitation and Computer Crime Unit of the Georgia Bureau of Investigation received a request for assistance from the Oconee County Sheriff’s Office in investigating multiple offenses. sex committed against children by Crooms, ”said GBI Deputy Special Agent Lindsay Marchant. A press release. “The investigation revealed that these crimes were allegedly committed in Newton County, Georgia, as well as in several different locations in the United States.”

In 2017, Crooms successfully asked a judge to remove his name from the sex offender registry despite Fultcher’s objections and his guilty plea.

“Their argument was that he was a changed man and that he was a model citizen who was out of trouble, hadn’t committed a crime since,” she said.

Fulcher believes the new charges show he hasn’t changed and should never have been taken off the sex offender registry or put back on the streets.

“I think our legal system has failed us,” she said. “I think once you’ve pleaded guilty to child rape, sexual assault charges, you shouldn’t get out of jail at all. You shouldn’t have a second chance.”

His removal from the sex offender registry meant he could travel freely with his wife, Rachel Overton, who the GBI said failed to stop the serial assaults.

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Immigrants Hope Registry saves immigration bill https://codogfederation.org/immigrants-hope-registry-saves-immigration-bill/ https://codogfederation.org/immigrants-hope-registry-saves-immigration-bill/#respond Wed, 22 Sep 2021 07:00:00 +0000 https://codogfederation.org/immigrants-hope-registry-saves-immigration-bill/ The American flag flies outside the United States Capitol. (Photo by Drew Angerer / Getty Images) Getty Images When the Senate parliamentarian told Democrats they couldn’t include their immigration provisions in a reconciliation bill, members of Congress and staff have turned to Plan B. This Plan B will likely include the “register”. What date of […]]]>

When the Senate parliamentarian told Democrats they couldn’t include their immigration provisions in a reconciliation bill, members of Congress and staff have turned to Plan B. This Plan B will likely include the “register”. What date of registration is chosen and whether the parliamentarian will allow its use in a reconciliation bill will affect the lives of millions of people. If done correctly, the registry could help applicants for employment-based immigrant green cards who have already entered and live in America.

“Senate MP Elizabeth MacDonough, a former immigration lawyer, shut down the possibility of granting 8 million people the right to apply for lawful permanent residence, determining in a notice on Sunday that she was not respecting the Senate rules for the budget reconciliation package because it was a policy change that went far beyond the budget, ”reported The hill. “The decision is critical because, under Senate rules, filibuster cannot be used to block a reconciliation plan, which means the policy changes included in the massive plan can become law if Democrats can get 50 votes from their own caucus in the Senate. While MacDonough’s ruling rules out the possibility of an easy legalization process for specific subgroups of immigrants, advocates are confident their saving arguments will sway MacDonough.

A likely “saving argument” for the parliamentarian is to change the registration date, an action that could benefit people here with legal status as well as those without status. Below is an overview of the most important issues regarding the registry.

How does the registry work? : The registry has been part of immigration law for almost a century. “The registry is a provision of immigration law that allows certain unauthorized aliens in the United States to acquire lawful permanent resident status,” explains the Congress Research Service. “He grants the Attorney General [now the Secretary of Homeland Security] the discretion to create a legal admission record for permanent residence for an alien who does not have such a record, resided continuously in the United States prior to January 1, 1972, and meets other specified requirements. The provision on the register has its origin in a law of 1929.

“The registry would help a whole bunch of people, and the only criteria would be that the person entered the United States on a particular date and resided continuously from that date in the United States,” the attorney said. Immigration Minister Cyrus Mehta in an interview. “They could apply for an adjustment of status and the government could impose additional fees or super-fees that would generate revenue for the United States. The person must also demonstrate good character and certain violations of criminal, smuggling, narcotics and other inadmissibility laws apply. Exemptions that exist under the INA [Immigration and Nationality Act] because these grounds for inadmissibility would apply even to a request for regularization at the registry.

“Unlike previous immigration provisions which were rejected by the parliamentarian, it is not necessary to establish that you entered the United States before age 18 or that you are an essential worker or that you have a petition I-130 or I-140 approved. A qualified candidate must prove that they entered the United States before the deadline, which is January 1, 1972, under current law [INA Section 249] and has resided continuously since that date.

Who would be included depends on the date: A report by FWD.us estimated that moving the registration date to January 1, 2011 would allow approximately 6.7 million people to be eligible for permanent residence.

If Democrats want to push back “amnesty” charges for moving the registration date to January 1, 2011, an argument could be made to move the date much closer to the present to help those in arrears on hold. legal immigration.

“I fully agree that the date will be postponed to January 1, 2021, so that the new provision can help as many people as possible who were waiting to either regularize their status or obtain a green card.” , Mehta said. “The fees that can be collected for each Section 249 adjustment request will generate billions of dollars in revenue for the treasury [depending on the fee set]. There are no quotas or ceilings for registered green cards. “

Would the parliamentarian authorize the registry? : “A simple provision simply modifying the date of registration and adding significant costs as a ‘tax penalty’ cannot be removed by the parliamentarian”, argues Leon Fresco, who previously worked in the Senate as the Director of Personnel of the Senate Judiciary Subcommittee on Immigration and Senior Advisor to Senator Chuck Schumer (DN.Y.). “This provision, if the fees are high enough, would in fact be the most deficit-reducing measure in the past two decades.”

Others are not so sure that the parliamentarian will approve the change of the registration date in a reconciliation bill. “It is difficult to say whether the parliamentarian will accept this alternative proposal,” said Cyrus Mehta. “She should do it this time because the Immigration and Nationality Law is not substantially changed and no new category is created in which people can apply for adjustment of status.” All that is happening is that the deadline will drop from January 1, 1972 to a more recent date. “

Another lawyer pointed out that the parliamentarian did not deny that there were financial advantages to including immigration measures in a reconciliation bill, but the parliamentarian said that the advantages inherent in legalization for individuals are more important. In other words, it was not a cost-benefit analysis but a cost argument. relative to the advantage, and assert the advantage [legalization] far outweighs the financial gain. In view of this argument, it is not clear whether changing the recording date would meet the parliamentarian’s standard.

Changing the recording date would benefit millions of people. If the date chosen was closer to January 1, 2021, it would cover people waiting for their family and work green card inside the United States.

(Update: On September 29, 2021, the parliamentarian of the Senate rejected the inclusion of an update to the date of the immigration register in a reconciliation bill. “The number of beneficiaries and the score of this amendment… are largely the same as those of the proposal to radically change the balance between politics and score, ”said the parliamentarian, according to the the Wall Street newspaper. The parliamentarian added: “The change of status in [lawful permanent resident] remains a change in circumstances throughout life, the value of which far exceeds its budgetary impact. “)



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The Motor Vehicle Register includes certain service options https://codogfederation.org/the-motor-vehicle-register-includes-certain-service-options/ https://codogfederation.org/the-motor-vehicle-register-includes-certain-service-options/#respond Mon, 20 Sep 2021 07:00:00 +0000 https://codogfederation.org/the-motor-vehicle-register-includes-certain-service-options/ Posted: Sep 20, 2021 / 11:37 AM EDT / Update: Sep 20, 2021 / 11:37 AM EDT SPRINGFIELD, Mass. (AP) – The Massachusetts Registry of Motor Vehicles resumed offering some services that had been suspended during the coronavirus pandemic on Monday. Twenty-one locations statewide will offer appointments for in-person vehicle and driver services, walk-in tours, […]]]>

Posted:
Update:

SPRINGFIELD, Mass. (AP) – The Massachusetts Registry of Motor Vehicles resumed offering some services that had been suspended during the coronavirus pandemic on Monday.

Twenty-one locations statewide will offer appointments for in-person vehicle and driver services, walk-in tours, and business-to-business transactions, which include wholesale transactions for car dealerships and sales agents. insurance, the agency said in an earlier statement.

Additionally, the Attleboro location will open for in-person services by appointment.

Walk-in services will be available at Braintree, Brockton, Danvers, Easthampton, Greenfield, Fall River, Haverhill, Boston (Haymarket), Lawrence, Leominster, Milford, New Bedford, Pittsfield, Plymouth, Revere, Springfield, Yarmouth, Taunton, Watertown, Wilmington and Worcester.

The agency still recommends making an appointment, and walk-in clients may have to either wait for assistance to be offered or return to a center on another date.

Also as of Monday, drop-off services that temporarily replaced in-person business-to-business services during the pandemic emergency will no longer be available.

Face covers are required at the Boston, Martha’s Vineyard, Nantucket, Easthampton, and Watertown locations as they are located in municipalities that currently have indoor mask mandates in place.


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Valley News – NHL unruly crowd forces DHHS to postpone vaccine registry hearing https://codogfederation.org/valley-news-nhl-unruly-crowd-forces-dhhs-to-postpone-vaccine-registry-hearing/ https://codogfederation.org/valley-news-nhl-unruly-crowd-forces-dhhs-to-postpone-vaccine-registry-hearing/#respond Wed, 08 Sep 2021 07:00:00 +0000 https://codogfederation.org/valley-news-nhl-unruly-crowd-forces-dhhs-to-postpone-vaccine-registry-hearing/ Editor’s Note: This story first appeared on New Hampshire Bulletin. The state Department of Health and Human Services abruptly postponed a hearing on proposed vaccine registry changes on Wednesday after losing control of the room to an unruly mob of vaccine opponents and activists privacy rights. Wearing “live free or die” shirts, renouncing masks and […]]]>

Editor’s Note: This story first appeared on New Hampshire Bulletin.

The state Department of Health and Human Services abruptly postponed a hearing on proposed vaccine registry changes on Wednesday after losing control of the room to an unruly mob of vaccine opponents and activists privacy rights.

Wearing “live free or die” shirts, renouncing masks and carrying “right to privacy” signs, nearly 150 people came to oppose what they see as an expansion of the vaccine registry. They got angry when the department tried to enforce the 95-person limit of the room and announced that the overflowing crowd would be waiting in the lobby for a turn to testify.

The presence of two security guards had no effect. The ministry’s offer to hold a second public hearing for those in the room was also not offered.

Even at 95 people, the small windowless auditorium was not an ideal setting for a public hearing as the state’s COVID-19 cases average 351 per day. It became more evident with almost no one wearing a mask and almost everyone singing, reciting the pledge of allegiance, and shouting at department officials.

Seventeen minutes later, Allyson Zinno, administrator of the department’s administrative rules unit, announced that the hearing would be rescheduled and held in a larger room. She did not give a date as the crowd cheered and demanded victory.

New Hampshire was the last state in the country to have a vaccine registry when it launched one in 2017. Given its controversial history, fierce opposition to proposed rule changes came as no surprise . In fact, the registry was delayed for two years due to objections to the ministry’s original rules about how people would choose to participate and what information would be recorded.

At the start of Wednesday’s hearing, Zinno said the rules do not extend access to the registry or create a vaccine passport. The crowd was not convinced.

The proposed rule changes are both small, such as clarified definitions, and more substantial, such as adding other health records to the registry and documentation when a person requests to be removed from the registry. The process for refusing to be included in the registry would remain the same: a health care provider must give a patient the choice to opt out.

The timing of the proposed changes is unclear.

The state is required to review administrative rules every 10 years, but may do so more frequently, the department said in response to questions from the Bulletin earlier this week. When asked if these proposed changes were related to COVID-19 or the vaccine, the department said in an email: “These rules apply to the administration of all vaccines, including the COVID vaccine. -19. ”

He continued, “The department can also update (rules) as often as there are changes needed.”

The ministry did not respond when asked to clarify whether the pandemic resulted in an early review of the rules.

The proposed changes would add a “medical screening record”. The ministry said this would include a history of illness.

“For example,” the ministry wrote in its email, “if someone has documented proof of chickenpox (chickenpox) immunity, they don’t need to be chickenpox immunity.”

Existing rules prohibit health care providers and the state from keeping track of a person’s decision to be removed from the register. That would change under the proposed rules.

The ministry said maintaining the record will allow the health care provider to ensure that patient information is not shared with the registry. It will also allow the state to remove someone from the registry and ensure that no patient information from other health care providers is included.

The ministry initially said it would take written public comments on the proposed changes until September 15. It was not clear on Wednesday whether he would extend the deadline once he announced a new date for the public hearing.


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