Medtrainer®: Healthcare compliance made easier
Spend less time on regulatory hurdles with Medtrainer, an affordable, easy-to-use learning management system (LMS) offering compliance management, staff training, credentialing and more.
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Regulatory updates
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How to address the top 10 F-tags in long term care & why compliance matters
Get insights on the top ten most commonly cited F-tags, including their causes and associated challenges, as well as potential solutions and tips to help you address F-tag compliance resolution.
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Is your home health agency ready for Medicare Advantage?
In this ebook, we explore steps home health agencies can take now to help prepare for new opportunities in the Medicare Advantage space.
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What long term care facilities should know about performance improvement for CMS surveys & beyond
As CMS surveys resume, find out how long term care facilities can use their COVID experiences as a catalyst for quality assurance and performance improvement.
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Value-based care trends to watch: 6 strategies to help your practice prepare
You may be wondering how to keep your practice competitive in the value-based care landscape. Here are some trends to watch and six strategies to help you prepare for this shift in care models.
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What DSCSA compliance means for non-acute care practices
Final Drug Supply Chain Security Act requirements take effect in November 2023. The last stage aims to track and trace drugs electronically through the pharmaceutical supply chain.
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How to prepare for a CLIA certification inspection
With strict standards of CLIA certification requirements, clinicians need to know how to best prepare for biannual inspections. Here's how labs can get ready.
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NHSN reporting requirements: Everything you need to know for 2022
Each year, the National Healthcare Safety Network (NHSN) updates its HAI data reporting requirements. Here's what you need to know for 2022.
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The new future of value-based care
Join as we deep-dive into the future of value-based care and telehealth with the Avalere team. We’ll explore how you should prepare for VBC models, as well as the continuing evolution of telehealth.
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Best practice guidelines on handling hazardous drugs under USP General Chapter <800>
Complying with USP General Chapter <800> requires guidelines on handling hazardous drugs and controlling occupational exposure to them in healthcare facilities. Here's what you need to know.
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CLIA 101: Answers to your most common questions about CLIA waived tests
What is CLIA and how does it impact your lab? Get answers to these and other common questions about CLIA waived tests for lab point-of-care testing and diagnostics.
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The Emergency Temporary Standard (ETS): A simplified review
OSHA’s Emergency Temporary Standard directive is designed to ensure uniform inspection & enforcement procedures to help protect healthcare workers from occupational exposures to COVID-19.
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How to avoid the most common OSHA violations & comply with the OSHA ETS
Help avoid the most common OSHA violations by following healthcare regulations and complying with the OSHA Emergency Temporary Standard.
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How to maximize home infusion reimbursement
How can home infusion pharmacies maximize home infusion reimbursement under Medicare Part B? Here are some tips from a longtime home infusion pharmacist.
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4 best practices for growing your business through better patient outcomes
Learn how value-based care can support patient outcomes, improve efficiency and support revenue growth through MACRA incentives.
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USP General Chapter <800>
U.S. Pharmacopeia's (USP) General Chapter <800> revised the standards for safe handling of hazardous drugs (HDs) to minimize the risk of exposure to healthcare personnel, patients and the environment.
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New blood pressure guidelines released
For the first time in more than a decade, the American Heart Association and the American College of Cardiology released new high blood pressure guidelines.
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PAMA lab reimbursement changes
Effective 2018, CMS has mandated new lab reimbursement rates in the Clinical Laboratory Fee Schedule (CLFS) under the Protecting Access to Medicare Act (PAMA).
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FDA flu reclassification
The FDA has reclassified rapid influenza antigen detection tests, mandating that visually read rapid flu tests must adhere to higher performance standards.
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AAMI ST79:2017
AAMI has released updated healthcare sterilization guidelines in the Comprehensive Guide to Steam Sterilization and Sterility Assurance in Health Care Facilities.
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