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Courses

  • 1 Request Info

    1-Day Seminar - HIPAA Training for the Practice Manager

    This one-day seminar will be addressing how medical practice managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, as there is so much misleading information regarding the do's and don'ts with HIPAA - I want to add clarity for specific to medical practice managers.
  • 2 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
  • 3 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.
  • 4 Request Info

    2019 HIPAA Audits & Enforcement Updates

    Overview: The collection of laws and regulations known commonly as HIPAA is comprised of two federal statutes and three federal rules: The Health Insurance Portability and Accountability Act of 1996 ("HIPAA"),the Health Information Technology for Economic and Clinical Health Act of 2009 ("HITECH"), the Privacy Rule (found at 45 C.F.R. 164.500 et. seq.), the Security Rule (found at 45 C.F.R. 164.300 et. seq.) and the Breach Notification Rule (found at 45 C.F.R. 164.400 et. seq.).
  • 5 Request Info

    3-Hour Virtual Seminar on Data Integrity and Governance for Computer Systems Regulated by FDA

    Overview Effective and compliant computer system data management is critical to organizations in the pharmaceutical, biologics, vaccines, tobacco, animal health, medical device or other FDA-regulated industry. During the past 30 years, best practices have been developed to ensure computer systems used in these environments can be cost-effectively managed while meeting all aspects of FDA compliance. To take this a step further, we are now looking at ways to ensure the data that resides on these systems is also managed in a compliant manner and one that will provide the best results for operations at the lowest cost.
  • 6 Request Info

    3-Hour Virtual Seminar on HIPAA vs. SAMHSA 42 CFR Part 2

    In this webinar the latest guidance from the US Department of Health and Human Services on harmonization of SAMHSA and HIPAA will be explained, We will discuss what qualifies treatment that falls under SAMHSA, HIPAA allows a number of disclosures, for treatment, payment, and healthcare operations purposes, without consent from the individual being treated, also We will examine how to deternmine if the services you provide place you under 42 CFR Part 2.
  • 7 Request Info

    3-Hour Virtual Seminar on Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences

    https://www.traininng.com/webinar/3-hour-virtual-seminar-on-japan---regulatory-filing-requirements-and-compliance-processes-for-life-sciences-200758live?channel=trainingregistry-april_2019_SEO
  • 8 Request Info

    3-Hour Virtual Seminar On The Anti-Kickback Statute and Stark II: Basis for An Action Under the Federal False Claims Act? - Your Organization May be a

    Overview: The session will provide an overview of the Federal Civil False Claims Act (FCA) and how it works, the prohibitions of the Anti-Kickback Statute (AKS) and the physician anti-referral law (known as Stark II), and their available safe harbors.
  • 9 Request Info

    3-Hour Virtual Seminar on The Interface Between Medicare and Medicaid, Anti-kickback Statute (AKS), Stark II and the Federal Civil False Claims Act (F

    Overview: Recent cases and/or enforcement actions involving the Federal Civil False Claims Act (FCA) as well as the Medicare-Medicaid Anti-Kickback Statute (AKS) and/or Federal Physician Self Referral Law (Stark II) raise serious concerns regarding compliance issues with the hospital, physician practices, and other healthcare entities.
  • 10 Request Info

    3-Hour Virtual Seminar on Writing Effective SOPs

    Overview: Every biopharmaceutical company has SOPs, and new staff members are told that the company "has to have them" and that each employee "has to follow them". But why do there have to be SOPs and why must we follow them as written? And how can we do this effectively? Perhaps if everything always executed as planned then we would not need procedures, but this is not the case in the real world. An SOP or Standard Operating Procedure is used to ensure business processes are well thought through, that each task in a process is performed the same way every time, and important data is recorded, along with errors or deviations so corrective action can be taken. Standard operating procedures used in combination with planned training and regular performance feedback lead to an effective and motivated workforce.
  • 11 Request Info

    Auditing Physician Contracts Under the New Stark Rules

    In this session Mr. Wolfe will provide an overview of the Stark Law, including its 2016 changes. He will also discuss best practices for auditing physician compensation 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. Healthcare reform has invigorated the government's focus on healthcare fraud, including enforcement of the Stark Law. Improper design and implementation of physician arrangements can result in penalties, denial of payments, and exclusion from federal health care programs. Thus, ensuring Stark Law compliance will be critical for medical groups, hospitals and health systems looking to manage areas of enterprise risk.
  • 12 Request Info

    Auditing Physician Contracts Under the New Stark Rules

    Overview: In this session Mr. Wolfe will provide an overview of the Stark Law, including its recent changes. He will also discuss best practices for auditing physician compensation 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.
  • 13 Request Info

    Baltimore Seminar on HIPAA Upcoming Changes

    This seminar will go into great detail about what is going on in the HIPAA Security/ Privacy world. I will discuss why the government is all of a sudden going full bore in demanding compliance. You will learn risk factors to avoid, best practices you should be doing, and how to be proactive in your efforts. In addition we are going to be discussing the methods in which patients can now sue under HIPAA and the steps they may be taking for civil remedy. On top of that what your practice or business needs to do so you can avoid the situation all together. I will explain what is involved in a HIPAA audit, how it is done, why it is being done, risk factors, how to avoid an audit altogether, and what to expect if audited (from real life experience). We will travel through time and see how the legislation has progressed, why it was benign somewhat in the past, and where we are now.... All the way from the inception in 1996 to the current Omnibus Ruling.
  • 14 Request Info

    CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA process

    Overview This presentation will cover the FDA regulations (21 CFR Subpart J) regarding CAPA, how CAPA should be integrated into other branches of your Quality Management System, how to best approach CAPA (including initiation, evaluation, and follow-up verification), examples of documentation you can use to fulfill the CAPA requirement, as well as tips and tricks to what FDA auditors will look for when they come to visit your site.
  • 15 Request Info

    Case Management's Role in Managing Third Party Payer Denials

    Case management, as a member of the revenue cycle team, plays a strategic role in the implementation of strategies aimed at reducing and/or preventing third party payer denials. Reducing and preventing denials requires proactive and hard-wired processes that engage the entire interdisciplinary care team. The causes of denials are complex and therefore require complex solutions. This program will review the causes of denials and key strategies for reducing and preventing them. Solutions will include key members of the interdisciplinary care team including physicians, physician advisors, case management leaders and case managers. Strategies for analyzing your denial rate will also be included. 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/Case-Management-s-Role-in-Managing-Third-Party-Payer-Denials-504198/DECEMBER-2017-ES-TRAININGREGISTRY
  • 16 Request Info

    Changes 2016 in HIPAA Privacy Security

    I have conducted over 400 risk assessments for business associates and covered entities alike as well as worked directly with the Federal government in terms of auditing. This seminar will go into great detail about what is going on in the HIPAA Security/ Privacy world. I will discuss why the government is all of a sudden going full bore in demanding compliance. You will learn risk factors to avoid, best practices you should be doing, and how to be proactive in your efforts. In addition we are going to be discussing the methods in which patients can now sue under HIPAA and the steps they may be taking for civil remedy. On top of that what your practice or business needs to do so you can avoid the situation all together.
  • 17 Request Info

    Clinical Documentation Improvement: Moving to Improve Patient Outcomes

    Overview: Achieving high performing quality focused patient centered cost-effective outcomes based clinical care requires a multidisciplinary approach to delivering patient care. Why should you Attend: Accurate reporting and reflection of patient outcomes is paramount to success and exceling under value-based healthcare delivery and reimbursement models. The accuracy and completeness of input consisting of documentation that best communicates the patient encounter including need for care, investigation, treatment and outcomes drives patient care quality outcomes. Healthcare facilities and physicians face major opportunity costs and hurdles without solid consistent communication of patient care. A major limitation under the theory of limited constraints related to achieving high performing quality patient outcomes is the quality of the documentation of communication of patient care.
  • 18 Request Info

    Clinical Research Seminar 2016: Current Regulations under FDA and HIPAA

    Overview: This two day seminar will provide the foundation for the application, concepts and theories of clinical research. Within the two days, attendees will learn about the historical evolution of research, current regulations and guidelines including the Common Rule, FDA regulations and HIPAA. We will discuss site and study staff responsibilities in the conduct and reporting of research, types of studies and the regulatory requirements that apply to different study designs. We will discuss a variety of research including genetic, drug, device, and studies that use off-site or community partners. Current examples will be used and the audience will be invited to share their experiences and information. Registration Link - http://bit.ly/2djQYsR-Human-Subjects
  • 19 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.
  • 20 Request Info

    Computer System Validation (CSV) for FDA-Regulated Computers

    FDA requires that all computer systems used to produce, manage and report on GxP (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. This webinar will leave you with the information needed to plan, execute and document a computer system validation effort that meets FDA compliance standards.