Healthcare - Medical Office Administration

Overview Effective presentation skills are crucial to a successful career. You need to know how to present your ideas, projects, strategies, plans, and products in front of an audience. While most people are probably used to giving presentations face-to-face, today's business world has gone almost entirely virtual. But that doesn't mean that you get a free pass out of doing your presentations. In fact, it's quite the contrary. Now you need to learn how to do it effectively in a virtual environment!

LEARNING OBJECTIVES • Understand human error: factors and root causes. • Understand the importance of human error reduction: regulatory and business. • Define the process to manage Human Error deviations. • Identify root causes associated to human error deviations. • Learn how to measure human error rates at your site. • Identify how to control human error and what I can do to support human reliability. WHO WILL BENEFIT • Training managers and coordinators • Operations • Manufacturing • Plant engineering • QA/QC staff • Process excellence/improvement professionals • Industrial/process engineers • Compliance officers • Regulatory/legislative affairs professionals • General/corporate counsel Use Promo Code SPRS20 and get flat 20% discount on all purchases. To Register (or) for more details please click on this below link: http://bit.ly/2TeStAa Email: support@trainingdoyens.com Toll Free: +1-888-300-8494 Tel: +1-720-996-1616 Fax: +1-888-909-1882

With all new events the FDA has stated that it “recognizes the significant public interest in cannabis and cannabis-derived compounds, particularly CBD.” However, there are many unanswered questions about the science, safety, and quality of products containing CBD. AREAS COVERED • Current events associated to cannabis • FDA, CANADA, and Europe regulations and standards • What does it mean for drug manufacturing sites? • Application from Pharma to Cannabis • Our role from GMP standpoint • Industry crossover WHO WILL BENEFIT • Training managers and coordinators • Operations • Manufacturing • Plant engineering • QA/QC staff • Process excellence/improvement professionals • Industrial/process engineers • Compliance officers • Regulatory/legislative affairs professionals • General/corporate counsel To Register http://bit.ly/2RRxuBu Email: support@trainingdoyens.com Toll Free: +1-888-300-8494 Tel: +1-720-996-1616 Fax: +1-888-909-1882

Learn the effective electronic patient engagement tools and comply with HIPAA rules. Register to this webinar. 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/Strict-HIPAA-Rules-for-Patient-Engagement-Social-Media-Websites-Email-and-Text-Message-508143/APRIL-2019-ES-TRAININGREGISTRY

Overview Good documentation practice (commonly abbreviated GDP, recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.

Firms exporting products from the U.S. are often asked by foreign customers or foreign governments to supply proof of the products' status as regulated by the FDA. An export certificate is a document prepared by FDA that has information about a product's regulatory or marketing status in the U.S.

Overview This webinar will give you the tools that you need to ensure that you understand data integrity issues and best practices for ensuring data integrity at your company.

This course will teach how to conduct a software validation program for medical devices containing software that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described.

Overview This training program will provide the regulatory requirements for complaint handling in the pharmaceutical & medical device industries. The course will touch on complaint sources and details will be furnished on the interrelationships regarding complaint handling and product recalls. The course will also include timeline requirements associated with adverse event reporting.

Learn how to use websites and social media for patient engagement in healthcare without violating HIPAA compliance. 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/HIPAA-Violations-Social-Media-Web-Sites-Patient-Reviews-Simple-Compliance-Steps-to-Avoid-Danger-508096/MARCH-2019-ES-TRAININGREGISTRY

Listen to this program to understand what you can and cannot do with regard to Marketing to Medicare and Medicaid Beneficiaries. Register for the webinar today. 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/Marketing-to-Medicare-or-Medicaid-Beneficiaries-What-You-Can-and-Cannot-Do-504719/FEBRUARY-2019-ES-TRAININGREGISTRY

Learn how to document the medical records to support medical necessity and how to avoid common errors that invariably trigger medical record audits. 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/Is-my-Documentation-meeting-Medical-Necessity-509484/JULY-2018-ES-TRAININGREGISTRY

Attend this webinar to learn how to reduce the risk of penalties in your practice and tips for avoiding breaches and learn about real-life HIPAA compliance issues. 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/Is-Your-Medical-Practice-HIPAA-Compliant-Requirements-for-Privacy-Security-and-Breach-Notification-508689/JUNE-2018-ES-TRAININGREGISTRY

In this webinar you will learn what a HIPAA security incident is and elements you need to have in your security incident report and response policy and procedure. 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/What-Is-a-HIPAA-Security-Incident-and-What-Should-You-Do-About-It-507409/JUNE-2018-ES-TRAININGREGISTRY

In this session, you will learn and see the 5 steps of HIPAA breach notification rule requirements of covered entities and business associates. 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/HIPAA-Breach-or-Not-How-to-Find-Out-What-to-Do-509196/JUNE-2018-ES-TRAININGREGISTRY

Attend this webinar to know how to handle HIPAA security incidents, breaches, and complaints and the Department of Health and Human Resources Investigations. 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/Road-to-HIPAA-Compliance-How-to-Handle-HIPAA-and-HITECH-Security-Breaches-Complaints-and-Investigations-506877/MAY-2018-ES-TRAININGREGISTRY

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

This webinar will benefit medical device companies planning to have a CE mark under the European Union Directive 93/42/EEC. We will discuss what is new in ISO 14971:2012 and help you avoid delays in obtaining or maintaining your CE mark for compliance to the Medical device Directive, EU Directive 93/42/EEC on Medical Devices. 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/ISO-14971-2012-Does-your-Current-Risk-Analysis-Still-Comply-with-your-CE-Mark-Requirements-507129/FEBRUARY-2018-ES-TRAININGREGISTRY

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

Attendees will receive knowledge on important and essential requirements related to Risk Management for potential pharmaceutical adverse effects. This webinar will provide basic understanding of requirements for REMS and steps to consider for implementation. 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/Implementation-of-Risk-Evaluation-and-Mitigation-Strategy-REMS-What-do-you-need-to-do-now-507343/DECEMBER-2017-ES-TRAININGREGISTRY