This site uses cookies to improve your experience. To help us insure we adhere to various privacy regulations, please select your country/region of residence. If you do not select a country, we will assume you are from the United States. Select your Cookie Settings or view our Privacy Policy and Terms of Use.
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Used for the proper function of the website
Used for monitoring website traffic and interactions
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Strictly Necessary: Used for the proper function of the website
Performance/Analytics: Used for monitoring website traffic and interactions
MIPS: Core Changes for Clinicians and Groups Stable Thresholds for Performance and Data Completeness: The performance threshold remains at 75%, and the data completeness threshold is also unchanged at 75%, providing stability for MIPS participants through 2028. CMS’s 2025 Final Rule introduces both challenges and opportunities.
Date required : January 1, 2028 Key takeaway : Stay tuned in the months ahead as the ONC considers requiring electronic prior authorization as part of integrated e-prescribing workflows. Date required : January 1, 2028 Key takeaway : This simple update will significantly enhance your roadmap.
billion by 2028. For example, healthcare organizations are uniquely incentivized to improve security with passwordless authentication based on the HIPAA compliance risks they face on a daily basis. There are four key trends to watch for as healthcare facilities work to improve their security posture.
– The best resource for monthly healthcare regulatory compliance updates. Compliance Updates: April 2024 Overlook: Licensure Compacts Other Legislation Board Updates Interstate Medical Licensure Compact (IMLCC): On March 21, 2024, Florida joined the IMLCC as the 42nd member jurisdiction via Florida Senate Bill 7016.
billion by 2028. Aaron is a Certified Information Systems Security Professional (CISSP) who has acquired a wide range of organizational, technical, and compliance knowledge, applying it within data center and financial institution services sectors. Without a doubt, the healthcare industry is growing and thriving.
Healthcare compliance is complex because there’s no single set of guidelines an organization can reference. Policy management software also helps manage compliance requirements, reduce potential risks, and improve organizational communication. What Is Healthcare Policy Management?
Bureau of Labor Statistics, it is estimated that occupations across life, physical and social sciences are expected to grow 7% by 2028. Director of Business Development at IQVIA The healthcare industry is no stranger to workforce shortages, and the pharmaceutical industry may be next to experience disruptions brought on by labor challenges.
Based on GHX’s internal statistics, up to 40 percent of a buyer’s time is spent on order processing and exception management, while one to three percent of total med-surge spend is wasted on missed contract compliance savings. The industry must collectively try to break free of the status quo. The ASC market is expected to grow to $59.3
Healthcare spending is projected to exceed $6 trillion by 2028 , largely driven by rising costs of care for an aging population and the growing number of Americans suffering from chronic physical conditions such as pulmonary disease, diabetes and hypertension. Sheila Talton, CEO of Gray Matter Analytics.
The new workplace labeling, hazard communication program, and additional employee training requirements for mixtures will not be enforced against employers until January 19, 2028.
Other health facilities will start at $21 per hour in 2024, reaching $25 per hour by 2027 for community clinics and by 2028 for other facilities. Statutory penalties apply when non-compliance is knowing and intentional. Large health facilities and clinics will see an increase to $23 per hour in 2024, reaching $25 per hour by 2026.Other
between 2021, and 2028. There are many risk management regulations and compliance standards in the life sciences industry that must be followed to successfully maintain business operations and ensure the safety of staff and product users. The life science sector is one of the country’s most lucrative industries.
Maintaining compliance with safety and quality standards is a significant issue in medical device manufacturing. Millions of dollars are lost by manufacturers every year due to regulatory non-compliance issues and related lawsuits. We continuously hear of infractions and warnings issued to companies for lack of regulatory compliance.
Its growth is expected to almost double by 2028. The problem with attempting to stay in compliance with the shifts in legislation is that it can become a full-time job on its own. And out-of-town guests often seek a spa day while on vacation in the state. Around the world, the med spa market was estimated to be worth about $19.3
Healthcare compliance is complex because there’s no single set of guidelines an organization can reference. Policy management software also helps manage compliance requirements, reduce potential risks, and improve organizational communication. What Is Healthcare Policy Management?
through 2028, outpacing the average projected growth in the gross domestic product (GDP) by 1.1 By 2028, the healthcare industry’s share of the economy is projected to increase to a whopping 19.7% As more new regulations are issued, payers may need to strengthen payment integrity strategies to ensure compliance.
Stage 5: Effective May 6, 2028 Four years following the publication of the Final Rule, the FDA will enforce premarket review requirements for moderate (Class II) and low-risk (Class I) IVDs (i.e., The FDA notes that it will continue to exercise enforcement discretion during the review of premarket submissions received by this stage.
This modification means that all IVDs, including LDTs, will be required to comply fully with FDA’s medical device regulatory requirements, including registration and listing, premarket review, post-market reporting requirements and compliance with the FDA’s Quality System Regulation ( 21 C.F.R. Part 820 ), unless they fall under an exemption.
If you already own or are considering buying land that is governed by a property owner’s association, or commercial or residential restrictions, ensure that the association is aware of and in compliance with such Acts.
The goal is for these Enhanced Services to be a covered benefit included in the MMCO premium starting in State Fiscal Year 2028. Level II HRSN services are paid for primarily through managed care, on a non-risk basis, through April 1, 2027, meaning that MMCOs will not be financially responsible if the costs for HRSN services exceed premiums.
A major justification for President Biden’s tax hike proposal is to shore up the tenuous finances of Medicare whose trust fund is forecasted to be depleted by 2028. Historically, it is the most prolific driver of family bankruptcy, and now it is on its way to bankrupting our country collectively.
Additional details are provided with respect to the validity of certificates and “sell-off” periods. The Proposal needs to be adopted by the European Parliament and the Council, and it might still undergo some changes in this process.
The vote occurred on 16 February 2023 following a plenary meeting of the European Parliament, and represents a significant step towards a formal extension of MDR and IVDR compliance deadlines for some device manufacturers. and 211.84). On 02 February 2023, FDA held a teleconference with the firm.
The vote occurred on 16 February 2023 following a plenary meeting of the European Parliament, and represents a significant step towards a formal extension of MDR and IVDR compliance deadlines for some device manufacturers. and 211.84). On 02 February 2023, FDA held a teleconference with the firm.
Level 2: When a simplified analysis of the EFRA inspection report is performed to evaluate compliance with the GMP requirements and may be adopted unilaterally by ANVISA. The classification criteria include: Serious deficiencies: Typically linked to non-compliance with critical items. Major deficiencies: Associated with major items.
Part D Medication Therapy Management Program. CMS proposes several changes to its medical therapy management (“MTM”) program to reduce eligibility gaps so that more Part D enrollees with complex drug regimens at increased risk of medication therapy problems would be eligible for MTM services.
Level 2: When a simplified analysis of the EFRA inspection report is performed to evaluate compliance with the GMP requirements and may be adopted unilaterally by ANVISA. The classification criteria include: Serious deficiencies: Typically linked to non-compliance with critical items. Major deficiencies: Associated with major items.
The states which have implemented payment parity laws include: Arizona. Alaska (for mental health services only). California. Connecticut. Illinois (expires Jan. Massachusetts (for mental health services only). New Hampshire. New Jersey. New Mexico. Oklahoma (effective Jan. Rhode Island.
These platforms could eliminate the need for ongoing updates, reducing compliance burdens while enhancing workflows and data-driven insights—an attractive option in an increasingly complex regulatory landscape. HTI-2 brings substantial changes, making compliance both a necessity and an opportunity for vendors that move quickly.
On the other hand, organizations that fail to meet these regulatory milestones risk more than fines for non-compliance; they risk losing market share to those who are compliant. The Future of Prior Authorization Until these new regulations are implemented, PA remains a significant pain pointespecially for providers in specialty disciplines.
Fifteen more Part D drugs are set to be published in 2027, followed by 15 Part D and Part B drugs, collectively, in 2028. Program Compliance. Drug manufacturers may also be assessed an excise tax between 65%-95% depending upon the number of days that the drug manufacturer is out of compliance. Negotiation-Eligible Drugs.
We organize all of the trending information in your field so you don't have to. Join 26,000+ users and stay up to date on the latest articles your peers are reading.
You know about us, now we want to get to know you!
Let's personalize your content
Let's get even more personalized
We recognize your account from another site in our network, please click 'Send Email' below to continue with verifying your account and setting a password.
Let's personalize your content