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Courses

  • 121 Request Info

    Webinar On Device Accessories - Understanding and Implementing the Final Guidance Document

    The classification of device accessories has a high visibility. For example, the 21st Century Cures Act, signed into law in December 2016, amends the FD&CA; to include accessory classification. It is very important, as a result, to apply the guidance document to your firm's products to determine if any of them are an accessory and as a result, ensure they meet the device regulations.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/DEVICE-ACCESSORIES-505201/AUGUST-2017-ES-TRAININGREGISTRY
  • 122 Request Info

    Webinar On Implementing Effective Safety Audits

    Nobody at your facility has been hurt in more than a year. Weekly inspection forms are returned with no non-compliances. Are the facility's safety plans really working that well or is it just luck? Conducting a safety audit is one of the proven ways to answer that question.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/IMPLEMENTING-EFFECTIVE-SAFETY-AUDITS-507553/AUGUST-2017-ES-TRAININGREGISTRY
  • 123 Request Info

    Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach 2017

    Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system. The various jurisdictions, however, deal with post-market device issues in many different ways. The quality management system, QMS, needs three interlocking process: complaint management, adverse event reporting, and recalls. These processes also have supporting QMS processes such as corrective action and design changes. Overarching the QMS processes are the regulatory requirements, usually involving record keeping and reporting. This workshop covers these primary and secondary QMS processes and analyzes them in terms of US, EU, and Canadian regulations.
  • 124 Request Info

    Webinar On Examining The Final Market Stabilization Rule: What's There, What's Not, And How Might It Work?

    On April 18, 2017, the Department of Health and Human Services (HHS) issued a final regulation designed to stabilize the Affordable Care Act's (ACA) individual and small group health insurance (SHOP) markets during continued discussions in Washington D.C. over the repeal and replacement of the ACA. These rules were designed primarily to calm the fears of insurers and prevent them from leaving the exchanges.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/EXAMINING-FINAL-MARKET-STABILIZATION-RULE-504197/AUGUST-2017-ES-TRAININGREGISTRY
  • 125 Request Info

    Webinar On Complying With the New CMS Emergency Preparedness Rule for Medicare and Medicaid Providers and Suppliers

    The CMS released its long-awaited final rule establishing emergency preparedness requirements for healthcare providers and suppliers participating in Medicare and Medicaid programs to ensure they are able to meet patient and resident needs during emergency situations. The regulation went into effect on Nov. 16, 2016, and Medicare and Medicaid participating providers and suppliers must comply with the new regulations by Nov. 16, 2017.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/CMS-EMERGENCY-PREPAREDNESS-RULE-506497/AUGUST-2017-ES-TRAININGREGISTRY
  • 126 Request Info

    HIPAA Breach Notification Rule - What you must do to comply

    OVERVIEW Final regulations for the new HIPAA Security Breach require much more than notifying individuals affected by a Breach of their Protected Health Information. Covered Entities and Business Associates first must follow and document a very specific process to determine if a Breach occurred. If no Breach occurred documentary proof must be kept for six years. If a Breach did occur timely notifications and other actions must be undertaken and documented. WHY SHOULD YOU ATTEND • Breaches and incidents that might be Breaches happen all the time! • More than 173,000 separate breaches of Protected Health Information (PHI) affecting less than 500 individuals were reported to the U. S. For more detail please click on this below link: http://bit.ly/2uaGkhB Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510
  • 127 Request Info

    Controlling Hazards in Spices : Basic Supply Chain Food Safety Control Requirements

    Overview With the finalization of the FDA’s FSMA Preventive Control Rules, new FDA outbreak testing technologies and increasingly complex supply chain controls, spices and other low moisture foods are becoming increasing identified as outbreak contributors. Spices are frequently found to carry salmonella, are full of physical adulterants, are often not identified as allergens, and may be impacted by lead and, when not carefully controlled throughout the supply chain, represent a bacterial growth potential that can end up in processed foods. Spice handling operations are subject to environmental facility controls, environmental sampling and test, process validation, Good Agricultural Practices (GAP), current Good Manufacturing Practices (cGPM), sanitary transportation rules, as well as packaging, labeling and other controls. For more detail please click on this below link: http://bit.ly/2ttPXYk Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515
  • 128 Request Info

    Project Management for Non-Project Managers 2017

    This two-day seminar will begin by laying the foundation for the subject by first defining what a project is and then discussing the unique roles that the project manager must assume along the length of any project. The Triple Constraint, the most fundamental of project management principles, will be explained in detail with examples and tools provided that can be used to integrate the principle into any project management process. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900996SEMINAR?trainingregistry-September-2017-SEO
  • 129 Request Info

    HIPAA – BYOD – what is new in 2017

    Overview The areas covered in this webinar will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT. I will uncover myths versus reality as it relates to this very enigmatic law based on over 600 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors. I will also speak about real life audits conducted by the Federal government (I’ve been on both sides of these audits), what your highest risks are for being fined (some of the risk factors may surprise you). For more detail please click on this below link: http://bit.ly/2qqJ8Zq Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510
  • 130 Request Info

    How to Deal With the Disruptive Practitioner

    Overview Disruptive activity by practitioners in the hospital takes many forms. When it happens, it is important that the hospital and/or the medical staff take appropriate steps to see that it does not affect patient care or disrupt operations. Why Should You Attend Hospital executives, medical staff officers, and peer review committee members and support staff should attend to learn how to deal effectively with the disruptive practitioner. You will also learn how to prepare for the day when it becomes necessary to terminate such a practitioner’s privileges and medical staff membership. For more detail please click on this below link: http://bit.ly/2rwgrde Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510
  • 131 Request Info

    Webinar on What All Providers Should Know About This Emerging Payment Model

    Overview: Bundled Payments are becoming more and more recognized as the preferred method of value-based reimbursement by CMS and several other commercial payers. In this presentation this type of payment method will be explained in detail and real-life examples will be given of how bundled payments actually work. In addition, providers will learn ways to optimize their performance under a bundled payment paradigm and how to negotiate bundled service agreements to their best advantage. Why should you Attend: It is critical for providers to understand the emerging CMS payment models and how these new reimbursement structures affect their organizations. Providers should attend this session to learn how to optimize their performance under a bundled payment paradigm and how to negotiate bundled service agreements to their best advantage.
  • 132 Request Info

    Structuring and Auditing Physician Employment Agreements: Key Legal Considerations

    Overview In recent years, the health care industry has seen unprecedented levels of physician employment. Structuring employment arrangements appropriately and periodically auditing implementation are critical in today’s challenging enforcement climate. Why Should You Attend As health care organizations and physicians develop employment arrangements, they must manage their compliance and enterprise risk by ensuring the employment is defensible under the Stark Law. Prior to moving forward with any employment arrangement, the parties should carefully evaluate whether the proposed structure and financial terms support compliance with Stark’s technical requirements and key tenets of defensibility so they will be prepared to mount a defense in the event the arrangement is ever challenged. For more detail please click on this below link: http://bit.ly/2qCSqgA Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515
  • 133 Request Info

    Webinar On 3 hours virtual seminar on: Healthcare Medical Software/Applications - Risks, Validation & Interoperability

    The complexity and expanding use of software outpaces what the industry understands and regulatory concerns. This creates challenges to the development of software programs, especially ones that can accommodate future designs and use. Regulations of Medical Device Data Systems (MDDS) lay out criteria for the lowest level of software regulation. Future criteria remain fluid based on changing technology and its likely evolution. In the meantime, providers and suppliers need to establish a regulatory compliant approach that can be adapted to future regulatory paradigms and initiatives.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/HEALTHCARE-MEDICAL-SOFTWARE-APPLICATIONS-507892/JUNE-2017-ES-TRAININGREGISTRY
  • 134 Request Info

    Webinar On The ABC's of Healthcare Reform: How to Be Successful Given the Changing Health Policy Landscape

    This webinar will provide an in-depth understanding of the future of healthcare reform and its implications. We will provide a comprehensive overview of payment and delivery system reform (key approaches to incentivize quality and value), and highlight the core drivers behind health reform, including healthcare consumerism, a focus on population health, stronger use of HIT data to drive improvements and better decision-making, and patient engagement.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/THE-ABC-HEALTHCARE-REFORM-502184/MAY-2017-ES-TRAININGREGISTRY
  • 135 Request Info

    Webinar On Understanding the Quality Indicator Survey Process (QIS), Quality Indicator Programs (QIP) and the processes and requirements of CMS for Fo

    Based on a 2010 survey 40 percent of the 15,000 long term care facilities failed to meet the bases of 42 CFR. This Webinar will focus on the opportunity for Food Service Operations to perform within the intended regulation, understand and interpret intent. This webinar may be used as a training tool for food service managers who want to perform higher in the (QIS), or who have failed in the past to implement CMS guidelines.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/QIS-QIR-CMS-FOOD-SERVICE-HEALTHCARE-502170/MAY-2017-ES-TRAININGREGISTRY
  • 136 Request Info

    HIPAA and The IT Manager Webinar

    Overview: This lesson will be going into great detail regarding you practice or business information technology and how it relates to the HIPAA Security Rule, in particular portable devices. Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to personal devices. I will uncover myths versus reality as it relates to this very enigmatic law based on over 1000 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain how patients are now able to get cash remedies for wrongful disclosures of private health information. More importantly I will show you how to limit those risks by simply taking proactive steps and utilizing best practices.
  • 137 Request Info

    2017 Webinar on Ransomware and HIPAA - Prevent, Prepare, Respond and Recover

    Overview: This course explains treacherous Ransomware threats attacking the Healthcare Industry and how to prevent, prepare for, respond to and recover from a Ransomware attack. It covers HIPAA Rules that apply to Ransomware, compliance with the HIPAA Rules and how to conduct a HIPAA Breach Risk Assessment to prove a Ransomware attack did not result in a Breach of Unsecured Protected Health Information (PHI) - a violation of the HIPAA Privacy Rule. Why should you Attend: Ransomware including new, more treacherous varieties used by cyber-criminals to attack the Healthcare Industry HIPAA Rules that apply to Ransomware attacks "Social Engineering" tricks criminals use to sneak Ransomware into Electronic Information Systems What to do if your organization suffers a Ransomware attack Best practices to: Prevent Prepare Respond Recover from Ransomware Attacks How to do a HIPAA Breach Risk Assessment to determine if a Ransomware attack resulted in a HIPAA Breach - or not - if the assessment
  • 138 Request Info

    HIPAA and Human Resources Webinar

    This lesson will be addressing what human resources managers need to know regarding health records of their employees. We will go through "do's and don'ts"and cover many frequently asked questions I have received through my 17-year career in HIPAA compliance. Human resources managers need to get their HIPAA house in order as this law is now fully enforced across the board and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017 and beyond. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain how individuals are now able to get cash remedies for wrongful disclosures of private health information. More importantly I will show you how to limit those risks by simply taking proactive steps and utilizing best practices within the HR department as a whole
  • 139 Request Info

    Webinar on How to Manage the HIPAA Business Associate Process

    Overview: The webinar will cover how to find out if business associates have the necessary technical, physical and administrative safeguards in place to protect shared protected health information. The webinar will address when a vendor becomes a business associate and how that relationship may change the dynamics. Understanding the Business Associate Agreement (BAA) process and making sure all ten government mandated requirements are in place will be covered. Find out about the use of Vendor Security Questionnaires and how to implement. The webinar will cover breaches caused by business associates and how to handle such an occurrence. If your healthcare organization needs to understand what your responsibilities are in managing business associates, please join us for this informative and interactive course
  • 140 Request Info

    2017 Webinar on Structuring and Auditing Non-Physician Practitioner Arrangements

    In this session Mr. Wolfe will provide an overview of the Stark Law, including its 2016 changes. He will also discuss best practices for negotiating and drafting NPP arrangements on behalf of health systems, hospitals, medical groups and physician practices. The webinar will focus on regulatory requirements, key provisions, valuation considerations and potential pitfalls that should be avoided. Why should you Attend: As health care organizations and physicians develop NPP arrangements, they must manage their compliance and enterprise risk by ensuring the their arrangements are defensible under the Stark Law. Prior to moving forward with any NPP arrangements, the parties should carefully evaluate whether the proposed structure and financial terms support compliance with Stark's technical requirements and key tenets of defensibility so they will be prepared to mount a defense in the event the lease is ever challenged.