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Courses

  • 941 Request Info

    What Contractors Need to Know About AIA A201 and Consensus Docs Contracts

    Overview: What are the top things you need to consider changing to standard construction contracts, as well as filling out the blanks correctly! Consequential Damages? Payment Terms? Project Financial Information, Termination? Dispute Mitigation Procedures? The answer is you need to be aware of all the top terms to stay on top of your game. Learn what changes other companies are generally making so you can keep up with the competition and some tips on how to stay ahead while still treating your contracting partners fairly. Why should you Attend: Standard contracts play a vital role in the construction industry, but how you use them can make or break your business. There are certain provisions that you absolutely need to pay careful attention to or change, including getting financial information, consequential damages, review of contract documents, termination and payment terms.
  • 942 Request Info

    What is 21 CFR Compliance | 21 CFR Part 11 Regulations 2018

    Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the FDA has stepped up 21 CFR 11 inspections that include CSV. This course will build on the Validation and 21 CFR 11 Compliance Basic Course, to give hands on experience on executing on the computer systems validation of a system, and to discuss related activities such as Validation Master Plan, Infrastructure Qualification, Project Management for Validation and Validation of Test Tools Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901540SEMINAR?trainingregistry-March-2018-SEO
  • 943 Request Info

    What is Leadership Management Academy 2017

    Why Should You Attend? By attending, you will take advantage of a great opportunity to advance as a manager to the next level! Too often, we focus on getting things done and results and miss working on our self-development. Let's face it: this is how we get paid yet this is also how we keep falling behind when it comes to our careers. It's time to get ahead! Don't miss an opportunity to advance as a manager again! We'll take you through peer discussions addressing leading and managing, integrating finance and quality, managing your time effectively, managing performance and managing up. Join us as we help you report back to your manager that "I'm ready to take the next step in advancing my management career!"
  • 944 Request Info

    What is the Government Looking for In a HIPAA Audit

    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 2016 and beyond. There are an enormous amount of issues and risks for covered entities and business associates these days. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor as well as working directly with auditors used by Health and Human Services and dispel myths vs realities. I will go over steps to take to avoid an audit or survive an audit. I have also served as expert witness on legal cases involving HIPAA violations, and I will thoroughly explain how patients are now able to get cash remedies for wrongful disclosures of private health information (which leads to more audits).
  • 945 Request Info

    What is the Government Looking for In a HIPAA Audit

    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.
  • 946 Request Info

    What to Expect in a Federal HIPAA Audit & How to Avoid Audit 2017

    I will be speaking to real life audits conducted by the Federal government for Phase 2 and beyond (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). It seems almost daily I am receiving calls from nervous practice managers and compliance officers all over the USA regarding a HIPAA audit letter or call they have received. This lesson will be addressing how practice/business 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 2017. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information all over regarding the do's and don'ts with HIPAA - I want to add clarity for compliance officers and practice managers
  • 947 Request Info

    What to Expect in a Federal HIPAA Audit & How to Avoid Audit 2017

    I will be speaking to real life audits conducted by the Federal government for Phase 2 and beyond (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). It seems almost daily I am receiving calls from nervous practice managers and compliance officers all over the USA regarding a HIPAA audit letter or call they have received. This lesson will be addressing how practice/business 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 2017.
  • 948 Request Info

    What you Need to Know about HIPAA Compliance

    Being in compliance with HIPAA involves not only ensuring you provide the appropriate patient rights and controls on your uses and disclosures of protected health information, but 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. This starts with the understanding the fundamentals of a HIPAA compliance program.
  • 949 Request Info

    What You Need to Know as a Business Associate about HIPAA and Health IT

    As defined by the Health Information Portability and Accountability Act (HIPAA), a Business Associate can be any organization or person working in association with or providing services to a Covered Entity who handles or discloses Protected Health Information (PHI) or Personal Health Records (PHR). With certain exceptions, a person or entity that creates, receives, maintains, or transmits PHI for a function or activity regulated by the HIPAA Privacy Rule for a Covered Entity is a Business Associate. The HITECH Act, a recent update made to overall HIPAA regulations require Business Associates to comply with HIPAA mandates regarding the handling and use of health information. As a Business Associate you must comply with a wide-range of regulatory obligations, including certain privacy obligations, security standards, and breach notification requirements.
  • 950 Request Info

    Why Good Risk Management is so Elusive

    Overview: Whether you are new to risk management or a seasoned veteran tuning up your risk program is constantly required. This program, "What good risk management is so elusive" is designed to make the process of risk management simple. This webinar will walk through the four core elements of a strong risk management program that everyone can understand and implement with little cost and effective measurable results. If you are interested in saving your firm money, reducing risk, and simplifying your risk program you must attend this webinar. The speaker uses stories to illustrate the four core elements in a fun and interesting twist on human nature to explain why "good" risk management is elusive.
  • 951 Request Info

    Why is FDA at my facility, and what do I do during an inspection 2017

    Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer. This presentation will review and emphasize the do's and don'ts and cardinal rules as to interviewing, how to respond, reviewing documentation, etiquette, use of certain words, body language, responding to questions/requests, etc., and certainly replying to 483's and Warning Letters. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900762SEMINAR?channel=mailer&camp=Seminar&AdGroup=trainingregistry_April_2017_SEO
  • 952 Request Info

    Winning Strategies for Dealing With Difficult People

    Advantage Legal Seminars is one of the leading providers of continuing legal education in the U.S. This program has been approved for CLE credits in many states.
  • 953 Request Info

    Workplace Violence Plans, Policies & Procedures for Hospitals & Healthcare Facilities

    How safe is your healthcare facility from workplace violence? Workplace violence against healthcare workers can be significantly reduced with a comprehensive violence prevention program. This webinar will outline common risk factors for violence, the basics elements of a violence prevention program and strategies for responding to violent events when they occur. The importance of training nurses and other healthcare workers in recognizing and managing aggressive behavior will be emphasized. This webinar, presented by a recognized expert on workplace violence prevention, will familiarize participants with the ways by which healthcare organizations can ensure physical safety for its employees by preparing in advance. Contact Info: Netzealous LLC -MentorHealth Phone No: 1-800-385-1607 Fax: 302-288-6884 Email: support@mentorhealth.com Website: http://www.mentorhealth.com/ Webinar Sponsorship: https://www.mentorhealth.com/control/webinar-sponsorship/
  • 954 Request Info

    Workshop On Quality Audits for the Medical Device Industry

    Quality audits are an important element in implementing and maintaining an effective Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure on effective QMS.Price:$1400.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link
  • 955 Request Info

    Writing and implementing effective SOP 2017

    An SOP is a meticulous step-by-step description of how to do a task that leave no chance for errors and divergence. Writing a good SOP is not an easy job. It requires a firm understanding of the task to be described, an ability to describe in specific unique to that laboratory. Writing, implementing, maintaining and assessing, revising an SOP are all different and necessary jobs. Many people must continuously be involved in these steps. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901140SEMINAR?trainingregistry-September-2017-SEO
  • 956 Request Info

    Writing and implementing effective SOP's 2017

    An SOP is a meticulous step-by-step description of how to do a task that leave no chance for errors and divergence. Writing a good SOP is not an easy job. It requires a firm understanding of the task to be described, an ability to describe in specific unique to that laboratory. Writing, implementing, maintaining and assessing, revising an SOP are all different and necessary jobs. Many people must continuously be involved in these steps. Even a standardized method, such as an ASTM or IP method, is insufficiently written to pass as a well-written and compliant SOP. The reasons why will be described, as will the steps needed to convert a standard method into an SOP Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900912SEMINAR?channel=mailer&camp=Seminar&AdGroup=trainingregistry_April_2017_SEO
  • 957 Request Info

    Writing for Instructional Design and Training Certificate

    Discover how to use rhetorical writing techniques to articulate your desired training outcomes effectively. Learn through hands-on practice how to write to clarify, simplify, illuminate, and explain. Hone your editing skills so that you can eliminate hyperbole and cut unnecessary words to manage participant cognitive load. Find out how to use tone, point of view, and personality to keep your audience actively engaged.