Read CNSC free pdf with mock exam to pass your exam

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Exam Code: CNSC Practice test 2022 by Killexams.com team
CNSC NBNSC Certified Nutrition Support Clinician

BNSC certification provides an avenue to demonstrate that you have attained the skills and knowledge necessary to provide quality nutrition support care. We have determined the body of knowledge needed to have an understanding of nutrition support and developed a fair and valid means to test care providers including physicians, dietitians, pharmacists, physician assistants, and nurses.

Certified professionals are recognized as quality providers of nutrition support by the public, their colleagues, other members of the healthcare team, and administrators. The Certified Nutrition Support Clinician ® (CNSC®) certification can provide job mobility, open up job opportunities, and, in some cases, lead to promotion and monetary gain.

Objectives of Certification
To promote enhanced delivery of safe and effective care through the certification of qualified clinicians in nutrition support by:

Recognizing formally those individuals who meet eligibility requirements of the National Board of Nutrition Support Certification, Inc. and pass the certification examination for nutrition support clinicians.
Encouraging continued professional growth in the practice of nutrition support.
Establishing and measuring the level of knowledge required for certification by a nutrition support clinician.
Providing a standard of minimum knowledge deemed appropriate for clinicians practicing nutrition support; thereby assisting the public, healthcare professionals, and employers in the assessment of nutrition support clinicians.

Nutrition Support is an inter-professional field. After conducting extensive research, NBNSC developed a new credential, the CNSC® that is fair and valid for all professional disciplines involved in nutrition support. The dietitians, nurses, pharmacists, physician assistants, and physicians who provide care share a common body of knowledge and expertise that NBNSC has captured in the new test format. The content of the test reflects the tasks that healthcare professionals provide on a daily basis.

I. Nutrition Assessment (32%)
II. Clinical Management (55%)
III. Process Management (3%)
IV. Professional Practice (10%)

NBNSC Certified Nutrition Support Clinician
Medical Certified download
Killexams : Medical Certified download - BingNews https://killexams.com/pass4sure/exam-detail/CNSC Search results Killexams : Medical Certified download - BingNews https://killexams.com/pass4sure/exam-detail/CNSC https://killexams.com/exam_list/Medical Killexams : UserTesting Helps Companies to Safely Test Health and Wellness Experiences with HIPAA-Compliant Feedback

SAN FRANCISCO--(BUSINESS WIRE)--Dec 13, 2022--

UserTesting (NYSE: USER), a leader in video-based human insight, today announced the availability of new test templates for the UserTesting® Human Insight Platform that help companies test health and wellness experiences in the wellness applications industry, pharmaceutical industry, and medical care facilities.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20221213005278/en/

As digital becomes a more widely used channel for customer interactions in the health and wellness industries, organizations need efficient strategies to gather customer feedback quickly, securely, and within compliance standards. UserTesting is HIPAA compliant, and the templates help companies securely gather valuable insights while adhering to regulations and requirements for data management of private health information. With human insights gathered from individuals who have opted-in to share their perspectives, organizations can quickly get real-world, real-time feedback to inform their design and development of health and wellness experiences.

Digital applications are flooding the healthcare and wellness industries. According to research, in 2021, there were more than 350,000 digital health apps available to consumers. However, only the top 110 health and wellness apps accounted for more than 50 percent downloads, while 83 percent of apps only accounted for less than 1 percent of downloads.

Further, the ONC 21st Century Cures Act Final Rule states that all Certified Health IT Developers must conduct real world testing. With access to the UserTesting Contributor Network, all companies that plan to build Certified Health IT can easily meet the requirements of demonstrating interoperability and functionality in real world settings and scenarios through the UserTesting Human Insight Platform.

To ensure a viable future and to drive continued growth, organizations need to provide customers with the best possible experiences across all channels. The UserTesting templates for healthcare and wellness experiences incorporate best practices for recruiting contributors, securing consent to discuss health-related topics, and gathering feedback within the bounds of HIPAA regulations.

This UserTesting template bundle is designed to provide health and wellness organizations with evaluations of patient portals, electronic health records and health and wellness apps; wearable device testing of fitness trackers, monitoring devices, and more; gathering patient experience feedback on in-person, telehealth, or long-term care experiences; and guidance on best practices for healthcare messaging comprehension.

Organizations can use UserTesting’s pre-built questions as-is or customize the templates to address their specific needs. Capturing feedback can be done by leveraging the UserTesting first-party, opt-in network of contributors or getting feedback directly from their own network of customers, partners, and employees.

“The emergence of promising technology for the health and wellness industries is significantly driving growth in this market. During digital transformation, it is paramount that organizations reflect on how new developments of digital apps or wearable devices are impacting their end users,” said Janelle Estes, Chief Insights Officer of UserTesting. “Having the human insight to help guide the design, development, and deployment of apps, devices, and patient interactions, while meeting regulatory standards, brings confidence and assurance to health and wellness organizations looking to uplevel their customer experiences.”

The new templates are focused on helping companies to test healthcare and wellness experiences and add to the more than 100 pre-built testing templates available on the UserTesting Human Insight Platform.

About UserTesting

UserTesting (NYSE: USER) has fundamentally changed the way organizations get insights from customers with fast, opt-in feedback and experience capture technology. The UserTesting Human Insight Platform taps into our global network of real people and generates video-based recorded experiences, so anyone in an organization can directly ask questions, hear what users say, see what they mean, and understand what it’s actually like to be a customer. Unlike approaches that track user behavior then try to infer what that behavior means, UserTesting reduces guesswork and brings customer experience data to life with human insight. UserTesting has more than 2,500 customers, including more than half of the world’s top 100 most valuable brands according to Forbes. UserTesting is headquartered in San Francisco, California. To learn more, visit www.usertesting.com.

View source version on businesswire.com:https://www.businesswire.com/news/home/20221213005278/en/

CONTACT: UserTesting, Inc.

Andy Dear

press@usertesting.com

KEYWORD: UNITED STATES NORTH AMERICA CALIFORNIA

INDUSTRY KEYWORD: OTHER HEALTH SOFTWARE NETWORKS INTERNET PHARMACEUTICAL TELEMEDICINE/VIRTUAL MEDICINE DATA MANAGEMENT TECHNOLOGY HOSPITALS HEALTH TECHNOLOGY BIOTECHNOLOGY HEALTH

SOURCE: UserTesting

Copyright Business Wire 2022.

PUB: 12/13/2022 09:00 AM/DISC: 12/13/2022 09:00 AM

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Copyright Business Wire 2022.

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Killexams : ABMS Names John H. Sudduth as its New Chief Information Officer

CHICAGO , Dec. 12, 2022 /PRNewswire/ -- The American Board of Medical Specialties (ABMS), the leading organization that oversees the standards for physician Board Certification in the United States, has named John H. Sudduth, CISSP, PMP as its new Chief Information Officer (CIO). 

In his role as CIO, Mr. Sudduth will oversee all aspects of the operations of the Information Services department. He will also support ABMS' strategic initiatives and provide guidance to Member Boards on their technology needs.

Mr. Sudduth previously served as CIO for a public utility, where he had oversight of the utility's information technology as it related to strategy, policy, support, and operations. In addition, he served on the Executive Team, which was responsible for developing and executing the organization's information technology strategic plan.

Mr. Sudduth also served as CIO for the Illinois Department of Public Health, where he was also responsible for developing and implementing the agency's information technology strategic plan. He leveraged modern technology to drive efficient health care outcomes by coordinating with public health agencies across Illinois. Mr. Sudduth utilized best practice Business Process Mapping methodologies to lead efforts to document and re-engineer business processes throughout the Agency.

Mr. Sudduth holds several technical and professional certifications, including Project Management Professional Microsoft Certified Information Technology Professional (Certified Information Systems Security Professional), and (Certified in Risk and Information Security Control).

Mr. Sudduth holds a Master of Science in Information System Security and a Bachelor of Science in Organization Behavior, both from Northwestern University in Evanston, IL.

About ABMS

Established in 1933, the American Board of Medical Specialties (ABMS) is responsible for the creation of standards overseeing physician certification in the United States. Dedicated to improving the quality of care to the patients, families and communities they serve, the 24 ABMS Member Boards develop educational and professional standards and programs of assessment to certify physicians and medical specialists. More than 940,000 physicians and medical certified are certified by one or more of the ABMS Member Boards in one or more of 40 specialties and 88 subspecialties. For more information about ABMS, visit abms.org or call (312) 436-2600.

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SOURCE American Board of Medical Specialties

Mon, 12 Dec 2022 03:24:00 -0600 en text/html https://markets.businessinsider.com/news/stocks/abms-names-john-h-sudduth-as-its-new-chief-information-officer-1031967265
Killexams : Medical Device Testing Market Set To Grow At The Fastest Rate- Time To Grow Your Revenue
(MENAFN- Market Press Release) December 9, 2022 12:06 am - Medical Device Testing Market with COVID-19 impact, By Services (Testing, Inspection , Certification), Sourcing , Technology (Active Implant, IVD, Orthopedic & Dental, Opthalmic, Vascular), Class, Testing, Region)

The global medical device testing market is expected to grow USD 11.8 billion by 2025, at a CAGR of 4.8% during the forecast period.

The harmonization of standards, growing consumption of medical devices in emerging countries, increasing need of validation and verification for medical devices, the imposition of rigorous government regulations, the growing trend of outsourcing medical device testing services and standards across medical devices are a few of the driving factors for the market. The COVID-19 outbreak in 2019 further accentuated the development of advanced low-cost medical devices. These devices need to comply with stringent regulations regarding medical devices, hence, manufacturers are investing heavily in testing their devices.

Download PDF Brochure @ Services, by service type held the largest share in the global medical device testing market in 2019
There is an increasing demand for TIC services in medical devices, owing to the rising demand for good quality and standard products across the industry. In the market, testing services ensure the products have met the required quality, safety, and performance regulatory standards. A few of the major examples of testing services are electromedical device testing, biocompatibility testing, clinical research services assessing the final product to investigate the faulty material, and testing the performance of medical devices and the electrical safety of devices. Testing services are carried out in laboratories and research sites. Testing services assist manufacturers in improving the marketability of their medical devices and in lowering costs in the pre-production phase (e.g. R&D, the selection of suppliers, etc. However, the Certification services tend to grow at a higher CAGR during the forecast period as certifications ensure that the manufacturers of the medical products have followed the standards and quality and safety norms during the production process.

Outsourcing, by sourcing type will grow at a higher CAGR during the forecast period
Many large firms are increasingly outsourcing medical device testing services as the increased regulations make it costly to conduct in-house tests, thereby helping firms reduce the overall cost of testing.
The demand for outsourcing TIC services to third-party vendors is increasing for technologies, such as active implant medical devices, owing to the capital-intensive nature of in-house TIC activities. However, the in-house sourcing type held the major share of the global medical device testing market in 2019.

Asia Pacific is projected to grow at the highest CAGR during the forecast period
The medical device testing market in APAC is growing rapidly because of the rising per capita income among the middle class. Moreover, there is growing consumer awareness regarding the importance of certification. The medical device testing market in India is projected to growing at the highest CAGR during the forecast period. North America, however, holds the largest share in the global medical device testing market as Strict regulations have been established by the governments to maintain quality and safety standards in the industry, which drives the need for medical device testing services in North America.

SGS (Switzerland), Eurofins Scientific (UK), Bureau Veritas (UK), Intertek (UK), TÜV SÜD (UK), and DEKRA (UK), Source Bioscience (UK), NSF International (US), BDC laboratories (US) and Surpass (US) are the key players in the global medical device testing market.

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Killexams : Camacho: Medical certification for disability update

Mabuhay and håfa adai! An individual applying for naturalization must appear for an interview. During this interview, the immigration officer will determine whether to grant or deny the naturalization application. There are three components of the naturalization interview: Review of the application, English examination and a civics test.

Twenty-six applicants recite their Oath of Allegiance as their final step to becoming naturalized citizens during a naturalization ceremony, presided over by Magistrate Judge Micheal J. Bordallo, at the District Court of Guam in Hagåtña on June 23, 2022. The event was held in celebration of the Juneteenth National Independence Day holiday, also known as Emancipation Day, which is traditionally observed on June 19.

The first component is a review of the naturalization application. The immigration officer will go through the naturalization application with the applicant to ensure that the responses are accurate. If there are any changes or errors in the application, the applicant has an opportunity to correct and update his or her application.

The second component is the English examination. In this component, the applicant reads a sentence in the English language and writes a sentence in English. The following applicants are exempted from the English examination: An individual who is 50 years or older and has been a lawful permanent resident for at least 20 years; or an individual who is 55 years or older and has been a lawful permanent resident for at least 15 years.

If the applicant qualifies for the exemption, the applicant can also request for a translator during the interview.

The third component is the civics test. In this component, the applicant must study 100 questions regarding the United States government and history. During the interview, the applicant will be asked 10 of those questions, and must get 6 questions correct.

If the applicant is 65 years or older and has been a lawful permanent resident for at least 20 years, then the applicant will be able to take a more simplified version of the test. Instead of studying for 100 questions, the applicant will only need to study a total of 20 designated questions.

For those individuals who have certain disabilities, such as hearing impairments or blindness, certain accommodations will be given to enable the individual to take the test. For example, I have accompanied clients who are blind or are deaf, and the immigration officers have accommodated.

In instances where an individual suffers from a physical, developmental or mental impairment that prevents them from demonstrating their knowledge and understanding of the English language and/or civics requirement, an individual may obtain a medical exception, by submitting a Medical Certification for Disability Exception Form.

In the past, a Medical Certification for Disability Exception was challenging to obtain. However, the U.S. Citizenship and Immigration Services recently revised the Medical Certification for Disability Exception Form. More importantly, on Oct. 19, USCIS announced an updated policy guidance to clarify and conform with the most accurate revision of the Medical Certification for Disability Exception Form.

A Medical Certification for Disability Exception Form must be completed and certified by a medical professional. According to USCIS, the revised form aims to reduce the burdens on both USCIS and the applicant “by eliminating questions and language that no longer have practical utility or were redundant.”

The revised form also gives the medical professional the option to “indicate an applicant’s need for an oath waiver, thereby eliminating the need for separate medical documentation.” Additionally, an applicant is able to submit the Medical Certification for Disability Exception Form even after the naturalization application is submitted.

An individual who suffers from a disability but can still complete the English and civics component of the interview with certain accommodations does not need to submit the Medical Certification for Disability Exception Form. The form is only for those individuals who suffer from certain disability and ailments, and who would not be able to successfully complete the English and Civics component of the interview.

For further questions or concerns on the Medical Certification for Disability Exception Form, or various immigration issues, a consultation with an experienced immigration attorney is recommended.

Catherine Bejerana Camacho is a Filipino-American attorney raised on Guam and licensed to practice in Guam and California. She specializes in employment and family-based immigration law, corporate law and family law.

Sat, 19 Nov 2022 22:45:00 -0600 en text/html https://www.guampdn.com/opinion/camacho-medical-certification-for-disability-update/article_7e7c886e-6870-11ed-a627-578e3a3c8624.html
Killexams : Benefits of ISO 13485 Certification for Medical Device Manufacturing

The medical device sector must meet stringent regulatory requirements plus convince potential customers that they make reliable, safe products. Having a strong commitment to quality can help customers achieve both those aims and others.

Parts of the ISO 13485 process involve identifying and documenting processes. For example, company representatives must find all processes that have even a minor connection to manufacturing. Next, they must create written procedures to establish which elements could introduce risks to the product.

Those threats could range from contaminated equipment to poorly trained personnel. After bringing attention to the risks, company representatives must name and describe measures to mitigate the potential issues.

ISO 13485 does not spell out the specific measures for device manufacturers to take. However, the certification gets people in the mindset that quality happens at every stage of manufacturing and that ongoing efforts enable maintaining high standards.

Reducing the Likelihood of Longstanding Issues

Another component of ISO 13485 requires ongoing managerial reviews to determine whether previously implemented controls work as expected or if further tweaks would get better results. Unfortunately, some leaders see these evaluations as box-checking exercises and feel under excessive pressure to get them done.

However, gathering relevant data and creating processes to keep that information up-to-date and accessible can make it easier to carry out thorough, non-rushed reviews related to ISO 13485. 

For example, looking at customer feedback, audit results, new regulatory requirements, and any details of corrective actions taken so far can help decision-makers verify whether quality controls related to ISO 13485 have the desired effects.

Additionally, these periodic reviews Boost the chances of catching issues that could lead to faulty products or operational efficiencies. They encourage better visibility that limits the likelihood of an unaddressed issue causing long-term problems.

Increasing Marketplace Competitiveness

The most accurate version of ISO 13485 requires that certified companies insist that any subcontractors conform to the standard, too. That means the commitment to quality extends beyond a particular organization. Many potential customers appreciate that, knowing that working with any new company poses challenges. ISO 13485 reduces many of them with its emphasis on quality.

Also, since ISO 13485 is an internationally recognized standard, it can help in cases where company leaders want to expand into other countries and boost their chances of success. Certification assists organizational leaders in conveying that they take quality seriously.

It’s vital to convince stakeholders of efforts to prioritize quality since medical devices directly affect people’s lives. Minimizing the chances of harm and increasing positive outcomes helps potential customers build trust in a company and decide it makes sense to work with or purchase from them.

Helping Products Stay on the Market Without Issues

Statistics indicate that approximately 4,500 medical devices and drugs get taken off the market owing to recalls. Just as managerial reviews of ISO 13485 processes can prevent persistent issues, a certified company is less likely to experience problems that lead to getting products pulled from shelves. In addition to the lost profits that such events cause, recalls can permanently damage the public’s reputation, making many people perceive a troubled brand as unsafe.

However, corrective and preventive actions get built into the ISO 13485 framework, helping company representatives identify and tackle problems faster than they otherwise might. It’s also advantageous that getting certified can help create and maintain a culture of personal responsibility within the organization.

Once an employee understands that a single missed step or ignored protocol could cause quality issues that affect a whole organization, they’ll likely become more conscious of their behaviors and choices made while working.

Plus, if a company does experience a recall, being ISO 13485-certified should make it easier to target where things went wrong and prevent future issues. Doing those things should bolster public trust and reassure people that a device manufacturer has its operations under control.

ISO 13485 Certifications Strengthens Medical Device Companies

The medical device sector is a high-pressure industry where people praise innovation as long as it doesn’t sacrifice user safety. Moreover, manufacturers must respond to demand spikes, as instances like the surge in ventilator needs during the COVID-19 pandemic showed.

Getting an ISO 13485 certification can help a company make positive, permanent quality and process improvements. Thus, representatives from certified companies often find that ISO 13485 contributes to organizational resilience. It’s not right for every organization, but the associated benefits make it well worth consideration.

Mon, 05 Dec 2022 10:00:00 -0600 en text/html https://www.plasticstoday.com/medical/benefits-iso-13485-certification-medical-device-manufacturing
Killexams : Medical certification now needed for commercial balloon pilots No result found, try new keyword!“So we’re already compliant with the new FAA requirement.” Balloon Fiesta spokesman Tom Garrity said a medical certification for pilots “was not something that was historically ... Thu, 17 Nov 2022 15:03:00 -0600 https://www.abqjournal.com/2550985/rule-affects-some-balloon-pilots.html Killexams : THE ACCREDITATION COUNCIL FOR MEDICAL AFFAIRS (ACMA) DEVELOPS FIRST EVER BOARD-CERTIFIED BIOLOGICS & BIOSIMILARS SPECIALIST (BCBBS) CERTIFICATION

NEW YORK, Dec. 6, 2022 /PRNewswire/ -- The Accreditation Council for Medical Affairs (ACMA) is launching a new Board Certification program focused on biologics and biosimilars. This is the first and only accredited board certification in the biologics and biosimilars arena.

THE ACCREDITATION COUNCIL FOR MEDICAL AFFAIRS (ACMA) DEVELOPS FIRST EVER BOARD-CERTIFIED BIOLOGICS & BIOSIMILARS CERTIFICATION

ACCREDITATION COUNCIL FOR MEDICAL AFFAIRS (ACMA) DEVELOPS FIRST BOARD-CERTIFIED BIOLOGICS & BIOSIMILARS CERTIFICATION

The Board-Certified Biologics and Biosimilars Specialist (BCBBS) program will accredit, and board certify healthcare professionals such as pharmacists (PharmDs), MDs, PhDs, and Medical Affairs/MSL professionals.  With accurate guidelines from Food and Drug Administration (FDA) and Heads of Medicines' Agencies (HMA) Biosimilar Working Group in Europe addressing biosimilars interchangeability, the need for education among the medical and scientific community is vital.

William Soliman, Ph.D., BCMAS, ACMA Founder and CEO, said, "The role that biologics and biosimilars play in the treatment of various chronic diseases is growing rapidly.  Helping both the healthcare and life sciences industry better understand appropriate clinical use of biologics and biosimilars will be key to successful long-term patient outcomes."

Currently, biologics and biosimilars board certification does not exist in the industry. The BCBBS certification will cover important syllabus such as regulatory and scientific concepts for biologics, real-world evidence, economic considerations, FDA resources including the Purple Book Database, and the future outlook on biosimilars. The program is self-paced and online to enable learners from around the world to enroll.

As analysts predict, the global biologics and biosimilars market will continue to grow to be a critical part of the healthcare industry. The expansion of biologic treatment options through market entrance of biosimilars across several therapeutic areas offer multiple advantages that will ultimately benefit patients and the overall healthcare delivery system. Understanding biologics and biosimilars in the medical and scientific community will help not only accelerate potential development of new treatments through advanced biotechnology capabilities.

About the Accreditation Council for Medical Affairs (ACMA) The ACMA is a global organization providing award-winning solutions for certification, training, analytics, and insights to support the healthcare and life sciences industries. From Medical Affairs to Market Access, Managed Care, and Market Research, ACMA is the standard in the industry for certifying and credentialing prior authorization and medical affairs professionals in over 80+ countries. To learn more, visit medicalaffairsspecialist.org.

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SOURCE Accreditation Council for Medical Affairs (ACMA)

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Killexams : Grenova Earns ISO 9001:2015 and ISO 13485:2016 Certification as Part of Its Mission to Manufacture Green Technology

Zebrafish infection models shed light on Shigella infection

In this interview, NewsMedical speaks with Professor Serge Mostowy and Sydney Miles about their research on bacterial infection, and, in particular, on Shigella Flexneri and enteropathogens.

Tue, 06 Dec 2022 23:51:00 -0600 en text/html https://www.news-medical.net/news/20221207/Grenova-Earns-ISO-90012015-and-ISO-134852016-Certification-as-Part-of-Its-Mission-to-Manufacture-Green-Technology.aspx
Killexams : VirtaMed and CICE to announce partnership for gynecological endoscopy certification

The CICE (International Center for Endoscopic Surgery) in Clermont-Ferrand, France, an internationally renowned endoscopic training center and the first in Europe to implement the European certification (GESEA), has inaugurated a training room using VirtaMed LaparoS™ Gynecological Laparoscopy and GynoS™ Hysteroscopy simulators.

CICE and VirtaMed will partner to integrate the VirtaMed mixed-reality simulators into the CICE training program, developing a comprehensive training approach with the goal to include more advanced and measurable surgical cases to Boost the quality of training and the skills transfer to the operating room.

The VR-enabled simulators allow surgeons to practice key surgical skills such as camera navigation, fluid management, safe exposure and resection of anatomical structures as well as handling of surgical complications. All this in a highly realistic, objective and stress-free training environment. 

We are very excited to collaborate with VirtaMed on the development of an advanced surgical training program for gynecology. We chose the VirtaMed simulators because they offer a training environment that is very close to what we experience in the operating room and at the same time it offers objective performance evaluation criteria,”

Professor Revaz Botchorishvili, Director of CICE

"Our team is looking forward to working with CICE. VirtaMed’s simulators are designed with the premise of teaching manual skills based on state-of-the-art learning psychology findings in a highly realistic environment. The collaboration goes well in hand with our efforts towards standardized and proficiency based training not only for novices but also for more advanced residents," explains Dr. Martina Vitz, Senior Vice-President Training and Education at VirtaMed. 

VirtaMed is the world leader in medical training using mixed reality simulators for minimally invasive diagnostic and therapeutic interventions in general surgery, OB/GYN, orthopedics, and urology. Combining virtual reality graphics with original instruments and anatomic models for realistic tactile feedback, VirtaMed partners with medical societies, such as the European Society for Gynecological Endoscopy (ESGE), and medical device companies.  

VirtaMed’s simulation platform offers unique features:

  • Compatibility with all VirtaMed training specialities
  • Possibility to switch between different modules in less than 1 minute
  • Reliability and robustness of Swiss engineering

VirtaMed's vision is to Boost the quality of medical care with state-of- the-art, virtual reality based medical training and education. For more information, visit www.virtamed.com 

Thu, 08 Dec 2022 03:28:00 -0600 en text/html https://www.news-medical.net/news/20221208/VirtaMed-and-CICE-to-announce-partnership-for-gynecological-endoscopy-certification.aspx
Killexams : kadara™ medical Bolsters Transgender And Non-Binary Healthcare Awareness During The Holiday Season And Beyond

LAS VEGAS, Dec. 1, 2022 /PRNewswire/ -- kadara™ medical, makers of premium, patient-centric trocar kits, and sets, launches an educational social media campaign to recognize and support the diversity of transgender and non-binary people. The goals of the campaign are to increase the visibility of gender-diverse people, open a supportive dialogue, illuminate the fact that no two gender affirmation journeys are alike, and bring elevated support to "new year's affirmations"—while bringing to light awareness of 'authentication of self' this holiday season.

A Device As Diverse As Its Patients

The advertising campaign, "A Device As Diverse As Its Patients" features five people with stories about their authentic, unique gender identity journeys. While reassuring transgender and non-binary individuals that there is no one path forward, the campaign also aims to educate medical professionals and the general population about the exceptional diversity of the LGBTQ+ community. Crow, one of the campaign models, shares their journey. "When I was young, I was taught that sex and gender were inextricably linked. Femininity was an exhausting daily performance that led to severe mental health struggles," says Crow. "Thanks to the trans visibility and trans community support, I was able to break free of these limiting beliefs and imagine new possibilities. Today, I identify as "non-binary". I see my gender as a creative process of self-expression that is responsive, emergent, and fluid."

Kadara Medical, which has a unique diamond-shaped trocar design to reduce discomfort during minimally invasive surgical procedures, has taken an inclusive, supportive approach to bioidentical hormone replacement therapy (BHRT), hormone replacement therapy (HRT), and hormone affirming therapy (HAT). At the same time, the company continues to emphasize that gender affirmation hormone therapy is a choice, not a certainty, among transitioning and de-transitioning persons. "At Kadara Medical, we champion individuality as an LGBTQ+ owned business. We recognize that we are an exceptional choice for some transgender and non-binary people—but not all. That said, we celebrate all. That's the difference between a corporation and a family-run business, as this is our family." said Jonathan Bergstrom, CEO of Kadara Medical.

Trocars have been traditionally used in hormone replacement therapy procedures and are becoming more commonplace as the demand for transgender and non-binary gender-affirming hormone therapies increase. Today, there are 1.6 million transgender people ages 13 and older and 1.2 million non-binary people in the United States.

Through research and focus groups, Kadara Medical discovered an alarming lack of access to gender-affirming healthcare, making it difficult for transgender and non-binary people to get quality care. Additionally, insurance often does not cover specialized care, making gender-affirming therapies expensive, sometimes prohibitively. Kadara Medical is a champion for the LGBTQ+ community in shining a rainbow spotlight on this under-served community, during the holiday season and beyond.

Kadara Medical is committed to expanding diversity training among medical professionals, furthering HAT, and increasing LGBTQ+ access to healthcare. From the campaign, "A Device As Diverse As Its Patients", three important messages have surfaced in the context of Kadara Medical: there is a great need to inform and educate medical practitioners on how to connect with their transgender and non-binary patients; affordability of therapies itself is essential to pass onto patients, and patient comfort delivered by Kadara's proprietary medical device design.

Kadara Medical is a world-recognized manufacturer of premium, comfort-designed disposable trocar kits and reusable trocar sets for all pellet therapy. FDA registered, ISO 13485 Certified for quality management systems, and queer family-owned, Kadara is a leading trocar supplier to medical professionals who offer hormone replacement therapy, for every letter as represented by LGBTQ+.

Media Contact: 
Nicole Bergstrom, General@kadaramedical.com, 7752974778, Fax 7752974776

Cision

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SOURCE Kadara Medical

Wed, 30 Nov 2022 22:07:00 -0600 en-US text/html https://www.yahoo.com/now/kadara-medical-bolsters-transgender-non-120700600.html
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