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Courses

  • 1 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.
  • 2 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
  • 3 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.
  • 4 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.
  • 5 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.
  • 6 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!
  • 7 Request Info

    Webinar on Sterile Medical Packaging Design – 7 Essentials

    Individuals responsible for medical packaging system design and validation are required to provide a safe and effective packaging system that can deliver the enclosed product to the end-user without incurring defect or risk to patient safety. The scope of this webinar is to provide those responsible for medical device packaging system design with some key best practices and insights for the design and development of the medical packaging system, sterile barrier system. ISO 11607 part 1 will be the focus, ISO 11607 Part 2, equipment and process validation, will not be addressed. The following seven design essentials will be presented and the author will provide her perspective on how these seven essentials are key to success and efficient time to market for your medical device.
  • 8 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
  • 9 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
  • 10 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
  • 11 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.
  • 12 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.
  • 13 Request Info

    Webinar on Effective Compliance Plans for Medical Managers

    you need a compliance plan? Reducing exposure to liability is one of the key reasons for implementing and maintaining a compliance plan. Having an "effective and active" compliance plan proves that a medical practice has made reasonable efforts to avoid and detect misbehavior, and that the requisite intent to commit healthcare fraud was not present, and thus, could reduce penalties if wrongdoing is found. 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/MEDICAL-COMPLIANCE-501213/JAN-2016-ES-TRAININGREGISTRY
  • 14 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
  • 15 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
  • 16 Request Info

    Webinar on Structuring Physician Recruitment and Non-Physician Practitioner Support Arrangements under the New 2016 Stark Rules

    In this session Mr. Wolfe will provide a general Stark Law overview. He will also discuss best practices for auditing existing recruitment arrangements and for implementing new Non-Physician Practitioner (NPP) support arrangements under the new 2016 Stark rules. 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/NEW-STARK-RULES-2016-501425/MAY-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Medicare Penalties and Incentives- 2016 Updates for Medical Practices

    Medicare has included both Penalties and incentives to encourage participation and correct report for multiple programs. This webinar will review the programs that are currently targeted for these actions.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/MEDICARE-COMPLIANCE-501448/MAY-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On OSHA's Final Rule to Protect Workers from Exposure to Respirable Crystalline Silica

    The final ruling for crystalline silica exposure has been released by the Occupational Safety and Health Administration (OSHA). The rule is expected to provide a net benefit of approximately $7.7 billion, annually through control of exposure and other provisions of the rule.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/OSHAs-FINAL-RULE-PROTECT-WORKERS-CRYSTALLINE-SILICA-501506/MAY-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On HIPAA Risk Analysis: Clarified, Explained, Demonstrated

    Jocelyn Samuels, the top Federal official in charge of HIPAA enforcement said, "The one critical thing covered entities and business associates must do to ensure compliance with HIPAA’s Privacy Breach, and Security Rules is a HIPAA Risk Analysis - a comprehensive and thorough approach to assessing and addressing the risks to all of the protected health information(PHI) they maintain."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/HIPAA-RISK-ANALYSIS-501472/JUNE-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Your need to see what? The Importance of Document and Record Control for Medical Devices

    To provide external bodies the evidence of compliance to regulations and conformity to other requirements, medical device organizations must establish, implement and maintain documented processes for document and record controls.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/DOCUMENT-RECORD-CONTROL-MEDICAL-DEVICES-501522/JUNE-2016-ES-TRAININGREGISTRY