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Courses

  • 1 Request Info

    Anatomy & Physiology - Online Course

    Accredited self-paced online Anatomy & Physiology course. This course combines an interactive study experience with the convenience of the Internet. Students can enroll at any time and complete the course at their pace. Start learning A & P today! College credit available for an additional fee.
  • 2 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
  • 3 Request Info

    Complaint Handling and Medical Device Reporting

    Complaints can be an early warning of issues with your products and customer problems. It is vital to have efficient and effective processes for managing, analyzing, trending, and reporting product problems. This webinar will cover the basics of complaint management and medical device reporting. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/COMPLIANCE-MANAGEMENT-MEDICAL-DEVICE-REPORTING-501323/MARCH-2016-ES-TRAININGREGISTRY
  • 4 Request Info

    Design of Experiments and Statistical Process Control for Process Development and Validation

    This course will present the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes. A practical approach with case studies and examples will be used, with theoretical information introduced only when necessary to understand an experiment. Examples from real processes and testing procedures will be used to present the student with examples that will be directly applicable to their work. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901327SEMINAR?trainingregistry-November-2017-SEO
  • 5 Request Info

    HIPAA Compliance for Small Healthcare Providers 2017

    Being in compliance with HIPAA involves not only ensuring that you provide the appropriate patient rights and controls on your uses and disclosures of Protected Health Information; but that you also have the proper policies and procedures in place. If audited or the subject of a compliance review, you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901282SEMINAR?trainingregistry-November-2017-SEO
  • 6 Request Info

    HIPAA Privacy and Security - Time to get Serious 2017

    This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced 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. There are an enormous amount of issues and risks for covered entities and business associates these days. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901044SEMINAR?trainingregistry-November-2017-SEO
  • 7 Request Info

    Medical Coding - Online Course

    Accredited self-paced online Medical Coding training. This course covers ICD-10, HCPCS, and CPT and is approved by the AAPC. Students can enroll at any time and complete the course at their pace. Begin learning Medical Coding today!
  • 8 Request Info

    Medical Records Seminars

    Stay current on existing laws and recent legislation that affect your daily operations. Choose from a variety of seminar topics. AAMA, AAPC, AHIMA, HFMA, NAB, NFLPN, NHA, and other continuing education credits can be obtained where applicable.
  • 9 Request Info

    Medical Records Teleconferences

    Stay current on existing laws and recent legislation that affect your daily operations. Choose from a variety of seminar topics. AAMA, AAPC, AHIMA, HFMA, NAB, NFLPN, NHA, and other continuing education credits can be obtained where applicable.
  • 10 Request Info

    Medical Terminology - Online Course

    Accredited self-paced online Medical Terminology class. This class combines an interactive study experience with the convenience of the Internet. Students can enroll at any time and complete the course at their pace. Begin learning Medical Terminology today! College credit is available for an additional fee.
  • 11 Request Info

    Online Webinar on Using an IQ / OQ / PQ Approach to Validating Medical Device Software

    This medical device software validation training will show how you can validate software using IQ / OQ / PQ methodologies, typically employed for medical device process validation. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/VALIDATING-MEDICAL-DEVICE-SOFTWARE-501258/FEB-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

    Overview Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal between the test method and the product or process it is designed to detect. For example, while a defect-free process is desirable, a test method must be reliable both in detecting defects and in not rejecting acceptable samples. Those who work with process optimization and validation focus on optimizing a process and reducing variability. For more detail please click on this below link: http://bit.ly/2qiWXEm Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510
  • 13 Request Info

    Top Violations of Law, Series Two: Understanding the Most Common Violations of Law against Physical Therapists

    Physical therapists are now a doctoral educated health care professional and serve an important role in helping patients in our aging society regain and maintain their physical abilities. In addition, they serve to rehabilitate sports and exercise enthusiasts from athletic injuries. Physical therapists provide a truly “hands on” relationship with the patient as they carry out their healing component of physical medicine. In addition, physical therapy modalities overlap with several other health care practitioners who use the identical billing codes to bill for their services, too. This patient relationship and billing practices places physical therapists in a unique position of vulnerability to claims of misconduct.
  • 14 Request Info

    Update on Global UDI Initiatives for Medical Devices

    Overview This webinar will provide updates on the progress of unique device identification regulations around the world, including the status of the FDA’s implementation, requirements for UDI in the new EU MDR, the NHS e-procurement and PEPPOL programs in the UK, and the development of initiatives in other countries including Australia, Canada, Japan and Asia. Unique identification and barcoding are neither new technologies nor innovative concepts. But incorporation of UDI into the medical device industry has been long discussed and planned and slow to be implemented.
  • 15 Request Info

    Webinar on 2018 CMS Nursing CoP Standards for Hospitals: Proposed Changes and Updates

    Training on latest updates on 2018 CMS Nursing CoPs for hospital and proposed changes in discharge planning and the Hospital Improvement Rule will be discussed. 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/2018-CMS-Nursing-CoP-Standards-for-Hospitals-Proposed-Changes-and-Updates-508803/APRIL-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On 3-hr Virtual Seminar: What to Expect in a Federal HIPAA Audit & How to Avoid a Federal Audit

    This webinar 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.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FEDERAL-HIPAA-AUDIT-AVOID-FA-501739/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on An Update on Discharge Planning Rules and Regulations for 2018

    This program will review the current rules and regulations from the Conditions of Participation for discharge planning. We will then discuss the most recent changes from the Medicare program and how they will impact the roles of the RN case manager and the social worker. We will review strategies for safely transitioning your patients across the continuum of care.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/An-Update-on-Discharge-Planning-Rules-and-Regulations-for-2018-509438/JANUARY-2018-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Avoiding Common Mistakes in Medical Device Human Factors

    With the recent finalization of the FDA guidance, Applying Human Factors and Usability Engineering to Medical Devices, device developers have a clearer picture of the expectations for human factors testing on devices for which they seek clearance or approval. However, attempting to meet the FDA expectations using the guidance alone often results in limited understanding and poor execution of human factors studies.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/AVOIDING-MISTAKES-MEDICAL-DEVICE-501849/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Challenges with the NOTICE Act and the MOON Form: Is your Hospital/CAH Facility Ready for the Upcoming March 8 Implementation

    CMS has recently posted its updated version of the Medicare Outpatient Observation Notice (MOON), a standard notice that all hospitals and critical access hospitals must provide to Medicare beneficiaries who receive outpatient observation services for more than 24 hours. All hospitals and critical access hospitals (CAHs) are required to provide the MOON beginning no later than March 8, 2017.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/CHALLENGES-NOTICE-ACT-MOON-FORM-502058/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Classifying Medical Devices - US and EU

    This webinar will detail the medical device classification process for the United States through the FDA and will overview the very complex process for medical device classification within the EU. Specifically, this webinar will provide detailed background into the process and will make clear some of the very complex terms and sub-processes associated with medical device classification. We will actually work through the classification process step-by-step for the US and will overview how the process is accomplished for the EU.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CLASSIFYING-MEDICAL-DEVICES-505796/MARCH-2017-ES-TRAININGREGISTRY