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Courses

  • 1 Request Info

    Webinar On How to Write HIPAA Policies and Procedures

    The webinar will explain for HIPAA covered entities and business associates the process of drafting, adopting and implementing HIPAA compliance policies. Writing a policy is easier than one may think. It is a three-step process: Researching, drafting, and revising. This webinar will teach you to ask questions, solicit help, collect samples, keep the principles of substance, organization, coherence, style and correctness in mind while you are drafting, send your draft out for review, incorporate comments, implement the policy and repeat as necessary.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-POLICIES-PROCEDURES-501977/DECEMBER-2016-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar On Implementation of Risk Evaluation and Mitigation Strategy (REMS) Programs in a Health System

    Pharmaceutical and biologic products may have adverse effects. This can be observed either in general or in specific patient populations. Adverse effects may be related to class and structure and may be observed after approval of the drug. Strategies must be in place if a pharmaceutical or biologic product is deemed to likely have or is observed to exhibit a harmful response in addition to the health benefit. To assure public safety, the FDA requires implementation of a plan designed to mitigate the risk. These plans are developed as part of a risk evaluation and mitigation strategy (REMS).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/REMS-HEALTH-SYSTEM-501984/DECEMBER-2016-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On HIPAA Breach Notification Rule - What you must do to Comply

    Breach notification to the individual and to the U.S. Department of Health and Human Services (DHHS) is a key component of HIPAA compliance. Failing to do it properly can result in a seven-figure civil money penalty and is one of the key issues that DHHS audits for in the ongoing Phase II audits.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/HIPAA-BREACH-NOTIFICATION-RULE-501973/DECEMBER-2016-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar On Are You Ready For The FDA's Mandate Requiring Electronic Submission Conformance to SEND and SDTM?

    In this course, we will examine the 'why' behind the mandate and how it can change the way therapies are being developed, leading to faster market delivery of better drugs. We will explore FDA's vision of having electronic access to all submission data in ways that are not currently feasible. The electronic standards for exchange of nonclinical data (SEND) and clinical data (SDTM), developed by CDISC, will be discussed, focusing on SEND.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/FDAs-MANDATE-REQUIRING-ELECTRONIC-SUBMISSION-SEND-SDTM-501623/AUGUST-2016-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps)

    This webinar will review and provide a practical approach to investigating and reporting complaints of adverse reactions related to HCT/Ps. The FDA has implemented a risk-based approach to the regulation under 21 CFR Part 1271 for HCT/Ps to prevent the introduction, transmission and spread of communicable disease.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/INVESTIGATING-REPORTING-CELLS-TISSUES-HCT-PS-501482/JULY-2016-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps)

    This webinar will review and provide a practical approach to investigating and reporting complaints of adverse reactions related to HCT/Ps. The FDA has implemented a risk-based approach to the regulation under 21 CFR Part 1271 for HCT/Ps to prevent the introduction, transmission and spread of communicable disease.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/INVESTIGATING-REPORTING-CELLS-TISSUES-HCT-PS-501482/JUNE-2016-ES-TRAININGREGISTRY