The AACC 2014 conference saw over 20,000 attendees and 700 exhibitors introducing new products and technologies. Many vendors held lectures and demonstrations of systems pending FDA approval. Abbott featured an RFID-based inventory management system and attached storage to existing analyzers. Accriva Diagnostics was formed from the merger of ITC Nexus and Accumetrics. Beckman Coulter, bioMerieux, CellaVision, and other vendors highlighted upgrades to existing systems as well as new offerings pending regulatory approval.
Mediland is a group of Laboratories and Pathologists headed by Mediland Diagnostic & research Institute. Promoted with as primary objective of establishing super specialty diagnostic centre for various disease diagnosis and management.
This PDF will discuss the key information that is required for a medical device 510k submission. The information presented in this PDF pertains to just one of the many best practices in a medical device 510K preparation and submission.
Webinar or Online Training on A comprehensive overview of 510(k) submissionComplianz World
Complianz World is a US based company, and a leading GRC training provider has announced to conduct
Webinar or Online Training on
A comprehensive overview of 510(k) submission
Ethocle Reports has published its latest Market Research Report on Transcatheter Heart Valves - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Waters analytical technologies enable laboratories to generate more information, complete analyses more rapidly and reduce overall costs throughout key steps in the agrochemical development workflow - including Synthetic Chemistry, Purification, Formulation, Trace Detection, Metabolite ID.
Mediland is a group of Laboratories and Pathologists headed by Mediland Diagnostic & research Institute. Promoted with as primary objective of establishing super specialty diagnostic centre for various disease diagnosis and management.
This PDF will discuss the key information that is required for a medical device 510k submission. The information presented in this PDF pertains to just one of the many best practices in a medical device 510K preparation and submission.
Webinar or Online Training on A comprehensive overview of 510(k) submissionComplianz World
Complianz World is a US based company, and a leading GRC training provider has announced to conduct
Webinar or Online Training on
A comprehensive overview of 510(k) submission
Ethocle Reports has published its latest Market Research Report on Transcatheter Heart Valves - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Waters analytical technologies enable laboratories to generate more information, complete analyses more rapidly and reduce overall costs throughout key steps in the agrochemical development workflow - including Synthetic Chemistry, Purification, Formulation, Trace Detection, Metabolite ID.
The FDA’s 510(k) process for medical devices is doing a lot of rounds in the news lately. This includes the FDA Commissioner Dr. Scott Gottlieb’s announcement on the renovation to the 510(k) program and two new pilot programs initiated by FDA: the Quality in 510(k) (“Quik”) Review and the Special 510(k) pilot programs. In this week’s blog, we are shedding some light on what you should expect from the Quik 510(k) and the Special 510(k) programs...
Extending the Depth of Coverage in SWATH® Acquisition with Deeper Ion Libraries SCIEX
When it comes to testing complex cellular samples, SWATH® Acquisition in combination with deeper ion libraries provides more reproducibly quantified proteins. Learn how to balance library generation with results required from SCIEX experts.
Did you know that between January and June of 2015, 69% of 510(k) applications were rejected their first time?
Even though there have been significant changes to the content required in a 510(k) submission since the agency released their guidance in 2005, this should not be the case.
So what can you do to better manage your team’s 510(k) expectations?
How can you piece together your submission in a way that’s least likely to be rejected?
Join us for this free, 60 minute webinar, presented by our guest Allison Komiyama, PhD, RAC, principal consultant at AcKnowledge Regulatory Strategies and a former FDA reviewer.
Allison will be sharing with you some of her insider tips and best practices so you have a better chance at receiving your clearance letter faster than your competitors!
(You can view the full free webinar here: http://www.greenlight.guru/webinar/fda-510-k-submission)
Specifically, you will learn:
-Insider tips, tricks and best practices to getting your device to market faster
-What exactly are the expectations for your 510(k)?
-What does the 510(k) timeline look like and how long is it going to take?
-How to avoid having your 510(k) rejected
-What happens to your 510(k) once it’s submitted to FDA?
-What does the 510(k) pathway really look like?
-How to prepare your 510(k) submission
In May 2022, the European In Vitro Diagnostics Regulation (IVDR) will apply in the world’s second-largest medical device market. The new Regulation will introduce major changes to how manufacturers obtain CE Marking and maintain access to the European market. Many companies have yet to prepare for compliance to these new requirements or organize their regulatory transition strategies. Oliver will present the ‘What will it take? Review IVDR readiness” to help you understand the scope of the new regulations.
This session took place live at the Greenlight Guru True Quality Virtual Summit, a three-day event for medical device professionals to learn to get their devices to market faster, stay ahead of regulatory changes, and use quality as their multiplier to grow their device business.
What You May Have Missed at AACC 2018 White Paper - Kalorama InformationBruce Carlson
Each year the American Association for Clinical Chemistry draws tens of thousands of lab professionals and in vitro diagnostic vendors to one place. Kalorama Information was there and noted major developments at the meeting in this White Paper. Major themes of scientific sessions, new products from lab and IVD vendors are included.
EUGM 2014 - Marco Brazzarola (Aptuit): Aptuit Compound Registration and Inte...ChemAxon
Aptuit Verona transitioned from a former Pharma R&D Center to an integrated Contracting Discovery & Development Organization (CDDO). This presentation will describe how we collaborated with ChemAxon and adopted their platform to implement a Compound Registration system, integrated within our Discovery Data Management ecosystem. It will highlight the benefits of ChemAxon model and toolkit for companies like Aptuit, needing rapid/agile responses to evolving business needs.
Roundup of This Year's AACC Meeting in AtlantaBruce Carlson
The American Association of Clinical Chemistry was held this year in Atlanta, GA. Kalorama was at the meeting and notes several developments, with a particular focus on point-of-care.
LIMS from WINGLO
Sample Tracking: LIMS allows for the tracking of samples throughout their lifecycle, from collection to analysis and storage. This helps in maintaining the integrity of data associated with each sample.
Data Management: LIMS facilitates the organization and storage of various types of data, including test results, experiment details, and sample information. It often includes tools for data analysis and reporting.
Workflow Automation: LIMS can automate and streamline laboratory workflows, reducing manual errors and improving overall efficiency. This includes automated scheduling, sample processing, and data validation.
Inventory Management: LIMS helps in managing laboratory inventory, including reagents, consumables, and equipment. This ensures that the laboratory has the necessary resources for experiments and tests.
Audit Trail: LIMS typically includes an audit trail feature that tracks changes made to data, ensuring accountability and compliance with regulatory standards.
Integration with Instruments: LIMS can be integrated with various laboratory instruments, allowing for direct data transfer and reducing the risk of transcription errors.
User Access Control: LIMS provides role-based access control, ensuring that only authorized personnel have access to sensitive data and functionalities.
Compliance and Reporting: LIMS helps laboratories adhere to regulatory requirements by providing tools for compliance monitoring and generating reports for regulatory submissions.
Overall, LIMS plays a crucial role in modern laboratories by improving efficiency, data accuracy, and compliance with industry regulations.
The FDA’s 510(k) process for medical devices is doing a lot of rounds in the news lately. This includes the FDA Commissioner Dr. Scott Gottlieb’s announcement on the renovation to the 510(k) program and two new pilot programs initiated by FDA: the Quality in 510(k) (“Quik”) Review and the Special 510(k) pilot programs. In this week’s blog, we are shedding some light on what you should expect from the Quik 510(k) and the Special 510(k) programs...
Extending the Depth of Coverage in SWATH® Acquisition with Deeper Ion Libraries SCIEX
When it comes to testing complex cellular samples, SWATH® Acquisition in combination with deeper ion libraries provides more reproducibly quantified proteins. Learn how to balance library generation with results required from SCIEX experts.
Did you know that between January and June of 2015, 69% of 510(k) applications were rejected their first time?
Even though there have been significant changes to the content required in a 510(k) submission since the agency released their guidance in 2005, this should not be the case.
So what can you do to better manage your team’s 510(k) expectations?
How can you piece together your submission in a way that’s least likely to be rejected?
Join us for this free, 60 minute webinar, presented by our guest Allison Komiyama, PhD, RAC, principal consultant at AcKnowledge Regulatory Strategies and a former FDA reviewer.
Allison will be sharing with you some of her insider tips and best practices so you have a better chance at receiving your clearance letter faster than your competitors!
(You can view the full free webinar here: http://www.greenlight.guru/webinar/fda-510-k-submission)
Specifically, you will learn:
-Insider tips, tricks and best practices to getting your device to market faster
-What exactly are the expectations for your 510(k)?
-What does the 510(k) timeline look like and how long is it going to take?
-How to avoid having your 510(k) rejected
-What happens to your 510(k) once it’s submitted to FDA?
-What does the 510(k) pathway really look like?
-How to prepare your 510(k) submission
In May 2022, the European In Vitro Diagnostics Regulation (IVDR) will apply in the world’s second-largest medical device market. The new Regulation will introduce major changes to how manufacturers obtain CE Marking and maintain access to the European market. Many companies have yet to prepare for compliance to these new requirements or organize their regulatory transition strategies. Oliver will present the ‘What will it take? Review IVDR readiness” to help you understand the scope of the new regulations.
This session took place live at the Greenlight Guru True Quality Virtual Summit, a three-day event for medical device professionals to learn to get their devices to market faster, stay ahead of regulatory changes, and use quality as their multiplier to grow their device business.
What You May Have Missed at AACC 2018 White Paper - Kalorama InformationBruce Carlson
Each year the American Association for Clinical Chemistry draws tens of thousands of lab professionals and in vitro diagnostic vendors to one place. Kalorama Information was there and noted major developments at the meeting in this White Paper. Major themes of scientific sessions, new products from lab and IVD vendors are included.
EUGM 2014 - Marco Brazzarola (Aptuit): Aptuit Compound Registration and Inte...ChemAxon
Aptuit Verona transitioned from a former Pharma R&D Center to an integrated Contracting Discovery & Development Organization (CDDO). This presentation will describe how we collaborated with ChemAxon and adopted their platform to implement a Compound Registration system, integrated within our Discovery Data Management ecosystem. It will highlight the benefits of ChemAxon model and toolkit for companies like Aptuit, needing rapid/agile responses to evolving business needs.
Roundup of This Year's AACC Meeting in AtlantaBruce Carlson
The American Association of Clinical Chemistry was held this year in Atlanta, GA. Kalorama was at the meeting and notes several developments, with a particular focus on point-of-care.
LIMS from WINGLO
Sample Tracking: LIMS allows for the tracking of samples throughout their lifecycle, from collection to analysis and storage. This helps in maintaining the integrity of data associated with each sample.
Data Management: LIMS facilitates the organization and storage of various types of data, including test results, experiment details, and sample information. It often includes tools for data analysis and reporting.
Workflow Automation: LIMS can automate and streamline laboratory workflows, reducing manual errors and improving overall efficiency. This includes automated scheduling, sample processing, and data validation.
Inventory Management: LIMS helps in managing laboratory inventory, including reagents, consumables, and equipment. This ensures that the laboratory has the necessary resources for experiments and tests.
Audit Trail: LIMS typically includes an audit trail feature that tracks changes made to data, ensuring accountability and compliance with regulatory standards.
Integration with Instruments: LIMS can be integrated with various laboratory instruments, allowing for direct data transfer and reducing the risk of transcription errors.
User Access Control: LIMS provides role-based access control, ensuring that only authorized personnel have access to sensitive data and functionalities.
Compliance and Reporting: LIMS helps laboratories adhere to regulatory requirements by providing tools for compliance monitoring and generating reports for regulatory submissions.
Overall, LIMS plays a crucial role in modern laboratories by improving efficiency, data accuracy, and compliance with industry regulations.
Kemwell biologics presentation bp April 2018MithaliRosario
Founded in 1980, Kemwell provides customized process/product development and manufacturing to biopharmaceutical organizations worldwide. Our facilities are located in Bangalore, India and were built with technical guidance from Boehringer Ingelheim, providing customers with state-of-the-art technology along with the benefit of cost-effective manufacturing.
The 15,000 sq. m. facility consist of a cGMP drug substance manufacturing facility with 2x2000L bioreactors and a sterile fill and finish facility for cGMP drug product manufacturing with a floor for process development laboratories to support production of protein therapeutics from mammalian-cell culture or microbial fermentation.
For over 30 years, Kemwell supported pharmaceutical companies with their development and manufacturing needs. We developed and manufactured drugs for some of the world’s top pharmaceutical companies including Bayer, GlaxoSmithKline, Merck KGaA, Novartis and Pfizer. In 2017, Kemwell sold its pharmaceutical business to Recipharm AB but continues to leverage its 30-year experience to provide biotech customers with cost-effective solutions.
Delivering Healthcare Solutions to Combat the Spread of COVID-19Cassia Networks
Learn how Cassia Networks' gateways and VivaLNK's continuous body temperature monitoring sensors are being used in hospitals and clinical centers in China to help fight the spread of COVID-19.
Caso Lixis HEC Endeavor. Estrategia de entrada al mercado europeo de equipamiento de Control de Calidad para la Industria farmaceútica. Por José-Manuel Benzanilla-Guarachi y Pablo Porolli.
Top 5 Trends from RSNA 2015 Day 1 | MD BuylineMD Buyline
Day 1 of RSNA 2015: Learn what the top trends were at the Radiological Society of North America (RSNA) annual meeting and scientific assembly for 2015; from the leader in healthcare supply chain management solutions, MD Buyline.
For the full article, visit http://www.mdbuyline.com/research-library/articles/top-5-trends-from-rsna-2015-day-1/.
Learn how Medtronic is replacing the 5388 and 5348 short-term pacemaker models by offering aggressive pricing coupled with rebates and trade-in values for the older external pulse generator devices.
For the full article, visit http://www.mdbuyline.com/blog/medtronic-external-pulse-generators-taking-advantage-rebate-trade-options./.
Five cost saving tactics for healthcare providers that lead to better outcomes on the income statement and individually can help providers with their bottom line, including reducing, reusing, refurbishing, reprocessing and reimbursement. For the full article, visit http://www.mdbuyline.com/blog/power-re/.
How prepared is your lab? Can it handle infectious diseases like Ebola? MD Buyline recommends certain instruments and pricing for point of care systems for bedside testing.
View the full article at http://www.mdbuyline.com/blog/contained-laboratory-ebola-infectious-disease-preparedness/.
NTI 2015 Day 1: Managing Drug Diversion, Non-Invasive Monitoring, Improving R...MD Buyline
Learn about the top trends from NTI 2015 Day 1 including three presentations that highlight the great work that can be achieved by empowering nursing staff to utilize various technologies through nurse-driven protocols and interventions; from the leader in healthcare supply chain management solutions, MD Buyline.
For the full article, visit http://www.mdbuyline.com/research-library/articles/top-trends-nti-2015-day-1/.
Streamlining the Hospital Supply Chain: Just What the Doctor Ordered | MD Buy...MD Buyline
As hospitals begin transforming to adapt to new healthcare initiatives, they are easing the pain by restructuring and streamlining supply chain operations. Learn how MD Buyline helps hospitals save money on purchased services and consumables in this feature, then visit www.mdbuyline.com for more information.
Sciencescape: Research Scientists Put a Twist on Social Media | MD BuylineMD Buyline
MD Buyline discusses Sciencescape, a research delivery and exploration service based in Canada which streams breaking scientific papers on over 50 million categories into a "Twitter" like tool. For more insights and medical device and technology research from MD Buyline, visit www.mdbuyline.com
Healthcare IT: The New Break-Even Analysis l MD BuylineMD Buyline
Mr. Laskaris, MD Buyline analyst, presented healthcare IT acquisition examples using the new break-even analysis at the Hospital Value Based Purchasing Summit.
Nurse Call - How Much Does a Nurse Call System Cost by Room? | MD MD Buyline
Find out how much a nurse call system costs hospitals by room. For more information on how MD Buyline helps hospitals save money with cost analysis, visit www.mdbuyline.com
Purchasers can often achieve savings from $117,000 to $140,500 off the vendor quotes for angiography systems. Savings can be considerably higher depending on the situation. Keys to success are creating a strong, united team approach, getting competitive bids and using a trusted resource to validate the financial and clinical status of your proposals.
Learn more about how MD Buyline helps hospitals save money on purchased services and consumables at www.mdbuyline.com
Hemodynamic and Physiological Monitoring Systems | MD BuylineMD Buyline
MD Buyline shares cost analysis and tips for negotiating competitive pricing on hemodynamic and physiological monitoring systems. For more information on how MD Buyline helps healthcare facilities save money by evaluating medical capital technology, visit www.mdbuyline.com
Pricing for Portable X Ray Units | MD BuylineMD Buyline
Pricing for portable X-ray systems varies, depending first on the technology segment (analog versus digital), then on the power rating of the unit’s chassis, and finally on the type and size of flat panel detector that is associated with the system. MD Buyline analyzes these systems and provides pricing analysis in this infographic. Learn more about how MD Buyline helps hospital systems save money at www.mdbuyline.com
The focus in the knee arthroplasty market is shifting toward personalized instrumentation, minimally invasive approaches, robotic assistance and implants designed for specific genders. Types of knee replacement procedures include total knee, partial knee (or knee resurfacing), and revisions with replacement components that include the femoral, tibial, and/or patella components. These components are designed to be cemented or non-cemented, and can include ceramic or non-ceramic inserts. Pricing for knee replacements shown below includes all components. Find more consumable benchmarks from MD Buyline at www.mdbuyline.com
Pricing for hip implants shown below includes all components, such as cemented and non-cemented, ceramic and non-ceramic. In the last couple of years, some of the focus has shifted to more personalized instrumentation, as well as a minimally invasive approach and robotic assistance. As with most consumable items, lower prices are usually achievable by standardizing on one vendor. Learn more about how MD Buyline helps hospitals with consumable price benchmarking, visit www.mdbuyline.com
Building the Case for Integrating the Surgical Services Suite l MD BuylineMD Buyline
In this presentation hosted by HFMA, clinical analysts from MD Buyline review the markets, technologies, costs, vendors, clinical outcomes, financial considerations and reimbursements for integrated ORs, hybrid ORs and intraoperative iMRI/iCT.
http://info.mdbuyline.com/l/18032/2013-11-12/d1hy9
Medical Supplies Budgeting and Consumable Price Benchmarking l MD BuylineMD Buyline
Webinar: Understanding the Impact of Consumable Costs that Exceed Their Medical Capital Investments presented by MD Buyline and hosted by HFMA.
MD Buyline's experts share examples of consumables in the clinical laboratory, reagent rentals, pulse oximetry, bronchial thermoplasty, temperature management and cardiac ablation.
http://info.mdbuyline.com/l/18032/2013-10-01/cbkcp
Vendor Highlights from the AHRA 2014 Conference l MD BuylineMD Buyline
MD Buyline's clinical analyst Lori Webb highlights vendor showcases from the AHRA 2014 Conference in Washington, D.C. Learn about medical imaging solutions from Agfa Healthcare, Carestream Health, Canon, Del Medical, Fujifilm, GE, Konica Minolta, Kubtec, Samsung, Shimadzu, Siemens, Swissray and Toshiba.
http://www.mdbuyline.com/research-library/articles/2014-ahra-annual-meeting-exposition-vendor-highlights/
AHRA 2014 Annual Meeting l MD Buyline's Breakout Session: Transitioning to Di...MD Buyline
MD Buyline, the leader of healthcare supply chain management solutions, presented Transitioning to Digital Radiography at the AHRA 2014 Annual Meeting in Washington, DC.
http://www.mdbuyline.com/research-library/articles/transitioning-to-digital-radiography-2/
Part One: 2014 Changes to Reimbursement | MD Buyline | InfographicMD Buyline
In our report “Reimbursement Opportunities and Challenges in 2014,” we identify the key services and technologies hospitals should focus on to maximize CMS reimbursement payments.
For more information, visit mdbuyline.com
CHAPTER 1 SEMESTER V PREVENTIVE-PEDIATRICS.pdfSachin Sharma
This content provides an overview of preventive pediatrics. It defines preventive pediatrics as preventing disease and promoting children's physical, mental, and social well-being to achieve positive health. It discusses antenatal, postnatal, and social preventive pediatrics. It also covers various child health programs like immunization, breastfeeding, ICDS, and the roles of organizations like WHO, UNICEF, and nurses in preventive pediatrics.
Leading the Way in Nephrology: Dr. David Greene's Work with Stem Cells for Ki...Dr. David Greene Arizona
As we watch Dr. Greene's continued efforts and research in Arizona, it's clear that stem cell therapy holds a promising key to unlocking new doors in the treatment of kidney disease. With each study and trial, we step closer to a world where kidney disease is no longer a life sentence but a treatable condition, thanks to pioneers like Dr. David Greene.
One of the most developed cities of India, the city of Chennai is the capital of Tamilnadu and many people from different parts of India come here to earn their bread and butter. Being a metropolitan, the city is filled with towering building and beaches but the sad part as with almost every Indian city
Medical Technology Tackles New Health Care Demand - Research Report - March 2...pchutichetpong
M Capital Group (“MCG”) predicts that with, against, despite, and even without the global pandemic, the medical technology (MedTech) industry shows signs of continuous healthy growth, driven by smaller, faster, and cheaper devices, growing demand for home-based applications, technological innovation, strategic acquisitions, investments, and SPAC listings. MCG predicts that this should reflects itself in annual growth of over 6%, well beyond 2028.
According to Chris Mouchabhani, Managing Partner at M Capital Group, “Despite all economic scenarios that one may consider, beyond overall economic shocks, medical technology should remain one of the most promising and robust sectors over the short to medium term and well beyond 2028.”
There is a movement towards home-based care for the elderly, next generation scanning and MRI devices, wearable technology, artificial intelligence incorporation, and online connectivity. Experts also see a focus on predictive, preventive, personalized, participatory, and precision medicine, with rising levels of integration of home care and technological innovation.
The average cost of treatment has been rising across the board, creating additional financial burdens to governments, healthcare providers and insurance companies. According to MCG, cost-per-inpatient-stay in the United States alone rose on average annually by over 13% between 2014 to 2021, leading MedTech to focus research efforts on optimized medical equipment at lower price points, whilst emphasizing portability and ease of use. Namely, 46% of the 1,008 medical technology companies in the 2021 MedTech Innovator (“MTI”) database are focusing on prevention, wellness, detection, or diagnosis, signaling a clear push for preventive care to also tackle costs.
In addition, there has also been a lasting impact on consumer and medical demand for home care, supported by the pandemic. Lockdowns, closure of care facilities, and healthcare systems subjected to capacity pressure, accelerated demand away from traditional inpatient care. Now, outpatient care solutions are driving industry production, with nearly 70% of recent diagnostics start-up companies producing products in areas such as ambulatory clinics, at-home care, and self-administered diagnostics.
Explore our infographic on 'Essential Metrics for Palliative Care Management' which highlights key performance indicators crucial for enhancing the quality and efficiency of palliative care services.
This visual guide breaks down important metrics across four categories: Patient-Centered Metrics, Care Efficiency Metrics, Quality of Life Metrics, and Staff Metrics. Each section is designed to help healthcare professionals monitor and improve care delivery for patients facing serious illnesses. Understand how to implement these metrics in your palliative care practices for better outcomes and higher satisfaction levels.
The Importance of Community Nursing Care.pdfAD Healthcare
NDIS and Community 24/7 Nursing Care is a specific type of support that may be provided under the NDIS for individuals with complex medical needs who require ongoing nursing care in a community setting, such as their home or a supported accommodation facility.
Antibiotic Stewardship by Anushri Srivastava.pptxAnushriSrivastav
Stewardship is the act of taking good care of something.
Antimicrobial stewardship is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), improves patient outcomes, reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms.
WHO launched the Global Antimicrobial Resistance and Use Surveillance System (GLASS) in 2015 to fill knowledge gaps and inform strategies at all levels.
ACCORDING TO apic.org,
Antimicrobial stewardship is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), improves patient outcomes, reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms.
ACCORDING TO pewtrusts.org,
Antibiotic stewardship refers to efforts in doctors’ offices, hospitals, long term care facilities, and other health care settings to ensure that antibiotics are used only when necessary and appropriate
According to WHO,
Antimicrobial stewardship is a systematic approach to educate and support health care professionals to follow evidence-based guidelines for prescribing and administering antimicrobials
In 1996, John McGowan and Dale Gerding first applied the term antimicrobial stewardship, where they suggested a causal association between antimicrobial agent use and resistance. They also focused on the urgency of large-scale controlled trials of antimicrobial-use regulation employing sophisticated epidemiologic methods, molecular typing, and precise resistance mechanism analysis.
Antimicrobial Stewardship(AMS) refers to the optimal selection, dosing, and duration of antimicrobial treatment resulting in the best clinical outcome with minimal side effects to the patients and minimal impact on subsequent resistance.
According to the 2019 report, in the US, more than 2.8 million antibiotic-resistant infections occur each year, and more than 35000 people die. In addition to this, it also mentioned that 223,900 cases of Clostridoides difficile occurred in 2017, of which 12800 people died. The report did not include viruses or parasites
VISION
Being proactive
Supporting optimal animal and human health
Exploring ways to reduce overall use of antimicrobials
Using the drugs that prevent and treat disease by killing microscopic organisms in a responsible way
GOAL
to prevent the generation and spread of antimicrobial resistance (AMR). Doing so will preserve the effectiveness of these drugs in animals and humans for years to come.
being to preserve human and animal health and the effectiveness of antimicrobial medications.
to implement a multidisciplinary approach in assembling a stewardship team to include an infectious disease physician, a clinical pharmacist with infectious diseases training, infection preventionist, and a close collaboration with the staff in the clinical microbiology laboratory
to prevent antimicrobial overuse, misuse and abuse.
to minimize the developme
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...ILC- UK
The Healthy Ageing and Prevention Index is an online tool created by ILC that ranks countries on six metrics including, life span, health span, work span, income, environmental performance, and happiness. The Index helps us understand how well countries have adapted to longevity and inform decision makers on what must be done to maximise the economic benefits that comes with living well for longer.
Alongside the 77th World Health Assembly in Geneva on 28 May 2024, we launched the second version of our Index, allowing us to track progress and give new insights into what needs to be done to keep populations healthier for longer.
The speakers included:
Professor Orazio Schillaci, Minister of Health, Italy
Dr Hans Groth, Chairman of the Board, World Demographic & Ageing Forum
Professor Ilona Kickbusch, Founder and Chair, Global Health Centre, Geneva Graduate Institute and co-chair, World Health Summit Council
Dr Natasha Azzopardi Muscat, Director, Country Health Policies and Systems Division, World Health Organisation EURO
Dr Marta Lomazzi, Executive Manager, World Federation of Public Health Associations
Dr Shyam Bishen, Head, Centre for Health and Healthcare and Member of the Executive Committee, World Economic Forum
Dr Karin Tegmark Wisell, Director General, Public Health Agency of Sweden
2. AACC 2014 Conference Overview
The AACC is the must attend show for medical laboratory scientists. Over 20,000 laboratory medicine professionals, hundreds of new products and 700 exhibitors attend this event.
The AACC 2014 introduced an Industry Workshop Theater and an OEM Lecture Series on the exhibit floor. Vendor sponsored mini- lectures were more predominate in the booths at this year’s exhibit; topics ranged from utilization and automation to laboratory quality management systems. Additionally, vendors held off-site open invitation lectures and live- streaming presentations for those who could not attend.
3. Vendor Highlights
Abbott
Abbott featured Inventory Manager, which uses RFID technology and current purchasing systems to automate the lab inventory monitoring, tracking, stocking and ordering processes. The solution works with the CELL-DYN Sapphire and Ruby, Abbott Prism and Molecular product lines along with non-Abbott products. Readers vary from wall, over- door or handheld scanners. The system was a few weeks from availability at the AACC 2014.
The Accelerator a3600 Automated Track System now attaches to the CELL-DYN Sapphire, providing multiple storage modules and is in agreement to add DiagnosticaStagoand Instrumentation Laboratory coagulation systems.
4. Vendor Highlights
AccrivaDiagnostics
Formed after ITC Nexus bought Accumetricsin August 2013, AccrivaDiagnostics will be headquartered in San Diego where Accumetricsis currently based.
Featured Systems:
•ITC Hemochronand Avoximetersystems
•AccumetricsVerifyNowsystem
•ITC IRMA TruPointblood gas analyzer, which was acquired by LifeHealthon July 28, 2014
(continued)
5. Vendor Highlights
Beckman Coulter
Beckman now offers connectivity for the DxHproducts, which will allow labs to connect up to three DxH800 analyzers to a DxHSlidemakerStainer. Connectivity will not be available for the DxH600. The new DxHConnected WorkcellSolution is pending FDA approval, but is available outside of the U.S., including Canada.
Beckman has stated they will continue the relationship with CellaVisionand make the new CellaVisionDM9600 available upon its FDA approval.
(continued)
6. Vendor Highlights
bioMerieux
BioFire, who joined bioMerieuxin January 2014, exhibited in a booth separate from bioMerieux.
bioMerieuxfeatured systems include:
•VIDAS 3 Immunoanalzyerwith full traceability and automation that is pending FDA approval with a possible approval date at the end of 2014. This is expected to replace the mini VIDAS and offer more automation and higher capacity.
•BacT/ALERT Virtuo, an automated blood culture instrument that will replace the BAC-T system, is currently pending FDA approval. The BACT/ALERT Virtuowill use new APB (adsorbent polymeric bead) bottles.
(continued)
7. Vendor Highlights
CellaVision
The new DM9600 Imaging System, which has received CE approval in Canada but is pending FDA approval in the U.S., was featured. It offers an updated RBC software to help break down cell morphology and is expected to replace the DM96 system, which will continue to be offered by Sysmexand Beckman as part of their hematology solutions.
(continued)
8. Vendor Highlights
ClemexIntelligent Microscopy (based in Canada)
The ClemexHemaCytoimaging system offers:
•WBC differential
•RBC characterization
•Platelet counting of peripheral blood
It will be available in several different configurations with the highest level being the HemaCytoPlus. The system is pending FDA approval with a possible 2015 approval date and pricing will range from $25,000 to $80,000.
(continued)
9. Vendor Highlights
DiagnosticaStago
Stago’sHettichWorkcellAutomation unit (a STA-R Evolution Plus with a HettichCentrifuge) was on display at the Hettichbooth this year. The unit will feature auto-loading and may be released as early as Q1 or Q2 2015. It is currently pending correlation. Once available, Stagowill have three options for their coagulation systems as stand- alone, on the automation line, both currently available or as part of the Hettichautomation.
(continued)
10. Vendor Highlights
Horiba
Horiba hopes to add the ABX PentraXLR hematology instrument to its family of hematology instruments once it receives FDA approval. The XLR is for mid-sized labs and will feature a reticulocyte parameter.
(continued)
11. Vendor Highlights
Instrumentation Laboratory (IL)
IL introduced their new corporate identity and logo now as part of the WerfenCompany. IL joins Biokit, iNovaand SysteLabas part of the WerfenCompany to strengthen their focus in in-vitro diagnostics, haemostatis, critical care and autoimmunity:
•BioKitfocuses on infectious disease and serology
•iNovafocuses on autoimmune testing
•Systelabfocuses on IVD
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12. Vendor Highlights
Orchard
Sequoia, Orchard’s newest software that was released Q1 2014, is designed for scalability and flexibility, targeting higher volume labs.
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13. Vendor Highlights
McKesson
McKesson Lab products received an uplift, upgrading to a 64 bit PC and receiving a new user interface. The affected versions include V14.7, 15.5 and 16. McKesson Lab is MU2 Certified (Meaningful Use).
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14. Vendor Highlights
MedicaCorporation
EasyCellhematology imaging system, which received FDA approval in 2010, was on display at the Medicabooth. EasyCellcan accept handwritten slides and uses non-oil objectives because oiling is done outside of the system.
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15. Vendor Highlights
Radiometer
Systems featured at the conference include:
•ABL90 with wireless connectivity has been available since May 2014.
•AQURE POC data management system, a connectivity software, is pending release possibly in Q1 2015.
•1st Automatic, a bedside positive ID system which was launched in June of 2013, now features additional software to automate the process at the point of care site.
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16. Vendor Highlights
Roche
Cobas8100 automated workflow system was launched at this year’s meeting:
•Expected for sale in the first half of 2015.
•Offers a single tube bi-directional transport and multilevel transport system with a workflow that allows you to run both single primary and aliquottedtubes.
•Automates the send-out process by alliquoting, bar-coding and capping tubes with screw tops.
CobasM 511 Hematology Analyzer powered by Blood Hound:
•Still in development.
•Featured as the Blood Hound at last year’s AACC as part of Constitution Medical Inc.’s booth in conjunction with the announcement of the acquisition by Roche.
Cobas6500 Urinalysis series:
•Not yet currently available in the US.
•Consists of the cobasu 701 urine microscopy analyzer and the cobasu 601 urine analyzer.
Cobasb 123 point of care blood gas system:
•The system is not yet back in production but a re-release is expected in 2015.
Cobasb221 blood gas system:
•Redesign added parameters, a micro sample mode, pH pleural fluid clearance and extended life expectancy of the components.
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17. Vendor Highlights
SCC Soft
SoftBI™ and SoftExpress®modules were introduced:
•SoftBI: Supports products that offer a business intelligence solution for productivity and efficiency analysis.
•SoftExpress: Lab outreach product that helps with customer relations management, data quality and inventory management.
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18. Vendor Highlights
Siemens
Siemens launched the ADVIA Centaur XPT Immunoassay System and the ADVIA Chemistry XPT system at the AACC this year. Both of these systems can be connected to the Aptioautomation line and a full rollout of the XPT is expected by November of 2014.
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The VersaCellX3, which launched in February, was also featured at the Siemens booth and can connect up to three instruments for sample routing, including a STAT/priority drawer with eight positions. Siemens also displayed the CS-5100, CS-2100 coagulation analyzers and CLINTEK-Novus Urine Chemistry Analyzer, which are not yet available for sale in the U.S., pending FDA approval. The CLINITEK Novus will be paired with the UF1000i Urine Sediment analyzer to form the CLINITEK AUWiPRO Automated Urinalysis System.
19. Vendor Highlights
Sysmex
The DI-60 Slide processing system includes the DI-60 Integrated Cell Image Analyzer.
CellaVisioncell imaging systems is still offered as a standalone to complement the hematology systems.
CyFlowflow cytometer, which was acquired as part of Partec, provides CD4+ T-cell and CD4% enumeration in HIV monitoring but is used only for research.
The XN1000i, for lower volume labs or physician office laboratory settings, is pending release in the next 30 days. It is a smaller version of the XN1000 and does not provide auto repeats or reflexing. Reticulocyte counts and BF measurements are optional.
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My SysmexTM Mobile Lab Assistant, a mobile lab assistant that displays real-time information and performance data, launched at the exhibit. It is due for release September 1, 2014. It will be available on a table computer and offers a 10-hour battery life. Purchasing the system will include the software license, service and hardware with an annual fee that will vary with the size and complexity of the facility.
20. Questions about the AACC 2014 Conference?
Please feel free to ask the analyst questions about the AACC 2014 Conference at your convenience.
Visit www.mdbuyline.com/contact-us or call 1-800-375-5463.
Maria Hernandez, MBA, BSMT (ASCP)
Clinical Analyst