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Courses

  • 81 Request Info

    Webinar On Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes

    Medical devices sold into the European Union (EU) must comply with the applicable medical device directives, EU laws similar to FDA's regulations. Medical devices declared compliant must bear a CE mark in order to be admitted to the 28 member countries comprising the EU. The market population of these 28 countries is 450 million people, exceeding the 420 million people served by NAFTA (USA, Canada & Mexico), so many companies have an interest in penetrating this market.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/MEDICAL-DEVICE-CE-MARK-QUALITY-SYSTEM-501782/OCTOBER-2016-ES-TRAININGREGISTRY
  • 82 Request Info

    Webinar On Auditing Clinical Trials for Good Clinical Practice (GCP) Compliance

    Audits from either regulatory bodies and/or the sponsor companies are usual during the development of a clinical trial. The results of an audit affect both, the site and the sponsor of the clinical study. Good preparation for an audit starts from the beginning of the trial by identifying the risks of noncompliance.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/AUDITING-CLINICAL-TRIALS-GCP-COMPLIANCE-501768/OCTOBER-2016-ES-TRAININGREGISTRY
  • 83 Request Info

    Webinar On Clinical Trial Cost Estimation

    In this webinar, we will cover ways to structure the trials so that it is possible to assign cost estimates to the necessary resources over the life of the trial and then estimate the necessary costs by month, year, and total. We will discuss where some of the problems are in getting reasonable estimates, where they can go wrong during the trial and some ways to manage them.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/CLINICAL-TRIAL-COST-ESTIMATION-501814/OCTOBER-2016-ES-TRAININGREGISTRY
  • 84 Request Info

    Webinar On MEDDEV 2.7.1, Revision 4 for Clinical Evaluation and the Latest 2016 Guideline: A Guide for Manufacturers and Notified Bodies

    This webinar will explore the key changes, discussing the new requirements and noting the main clarifications within the guidance document. It will highlight the areas for you to be aware of and consider when conducting clinical evaluations.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/CLINICAL-EVALUATION-LATEST-2016-GUIDELINE-501774/OCTOBER-2016-ES-TRAININGREGISTRY
  • 85 Request Info

    Webinar On How to Conduct an Effective Annual Product Quality Review

    This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe. It will also discuss the comparative evaluation about similarities and differences of requirements associated with the manufacturing of the drug product in different countries.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/EFFECTIVE-ANNUAL-PRODUCT-QUALITY-REVIEW-501733/OCTOBER-2016-ES-TRAININGREGISTRY
  • 86 Request Info

    Webinar On GCP: The IND, How to Gain Approval for Clinical Trials in the USA

    Conducting a clinical trial with a drug that is not FDA approved or that is being used in an investigational manner can be daunting. The regulations governing such add to the complexity. When Good Clinical Practices are followed, the data is not only shareable amongst those who subscribe to GCP but it also helps provide a roadmap for conducting the trial.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/GCP-IND-CLINICAL-TRIALS-USA-501706/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 87 Request Info

    Webinar On 2017 Proposed Home Health PPS Rule:Pre-Payment Review and Other Regulatory Developments

    Home Health Services are undergoing increased scrutiny from CMS, the OIG and other agencies. To ensure your organization's compliance, it is important to know what changes are being proposed and what their impacts are on your organization.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/2017-HOME-HEALTH-PPS-RULE-501710/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 88 Request Info

    Webinar On Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products

    Effective and compliant computer system validation is critical to any FDA-regulated organization, including those manufacturing, testing and distributing tobacco products. During the past 30 years, best practices have been developed for other FDA-regulated industries to ensure that the cost of building and managing a computer system validation program for this purpose, along with the necessary policies and procedures.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/LEGAL-REGULATORY-POLICY-VALIDATION-FDA-501540/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 89 Request Info

    Webinar On How to Avoid PHI Breaches and HIPAA Violations While Doing Patient Engagement through Websites, Marketing and Social Media

    We all know the Internet is open for all to see. This includes the U. S. Department of Health and Human Services (HHS) and State Attorney General enforcement agents. A covered entity's breach for all to see! Misuse of social media, websites, or marketing can lead to HIPAA violations, lawsuits, and loss of patients and revenue.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/PHI-HIPAA-WEBSITES-MARKETING-SM-501701/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 90 Request Info

    Webinar On Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs

    This program will cover in detail the CMS regulations and interpretive guidelines for medical records. This is an extremely important section and includes hot issues like verbal orders, history and physicals, organization of the department, standing orders, discharge summaries, medication orders, and more.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-RECORD-STANDARDS-501593/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 91 Request Info

    Webinar On Defining and Managing Protocol Deviation/Violation/Exception

    Audits from either regulatory bodies and/or the sponsor companies are usual during the development of a clinical trial. The results of an audit affect both, the site and the sponsor of the clinical study. Good preparation for an audit starts from the beginning of the trial by identifying the risks of noncompliance during the trial. The first step in this process is understanding, correcting and preventing protocol deviations and violations.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/PROTOCOL-DEVIATION-VIOLATION-EXCEPTION-501703/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 92 Request Info

    Webinar On Unconscious Bias in the Workplace: How to Recognize and Diminish its Impact in Discrimination, Hiring, Promotions, & Retention

    From an individual standpoint, each of us should have an understanding of our biases so we treat others based on who they are rather than on stereotypes that we carry about various groups. From an organizational viewpoint, understanding unconscious bias is critical to strategizing ways to minimize it in the workplace to ensure a fair and discriminatory work environment. When unconscious bias is reduced, it enhances the organization climate. Unconscious bias has been recognized as a form of discrimination and can therefore lead to lawsuits.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/UNCONSCIOUS-BIAS-WORKPLACE-501668/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 93 Request Info

    Webinar On Trial Master File (TMF): FDA Expectations from Sponsors and Sites

    This webinar will help participants learn what is required of a Trial Master File for a clinical trial, and will acquire a practical understanding of how these documents provide evidence for the regulated activities of the investigator and the sponsor. Also, Attendees will learn which documents are essential, and which ones are not necessary in the event of an FDA audit.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/TRIAL-MASTER-FILE-FDA-EXPECTATIONS-SPONSORS-SITES-501613/AUGUST-2016-ES-TRAININGREGISTRY
  • 94 Request Info

    Webinar On EHS Incident Prevention - Proactive EHS Programs

    This training program will offer participants an understanding of the importance of recognition of hazards, and potentially unsafe conditions before serious EHS incidents and events occur. The course will focus on EHS incident prevention and creating proactive EHS programs.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/EHS-INCIDENT-PREVENTION-501557/AUGUST-2016-ES-TRAININGREGISTRY
  • 95 Request Info

    Webinar On Understanding the CMS' Merit-based Incentive Payment System (MIPS): Are you ready for performance-based Medicare reimbursements?

    The CMS Quality Payment Program is out and there are many updates that will significantly affect providers. Providers will be required to pick one of the two paths: The Merit-Based Incentive Payment System or the Advance Alternative Payment Models. This webinar allows you to understand more about the Merit-Based Incentive Payment System and its effect on your Medicare reimbursements.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/CMS-MERIT-BASED-INCENTIVE-PAYMENT-SYSTEM-501660/AUGUST-2016-ES-TRAININGREGISTRY
  • 96 Request Info

    Webinar On 2016 New CMS CoP Regulations for Managing Grievances and Complaints: What Hospitals Should Know about the CMS and Joint Commission and DNV

    Most of the hospitals in the US that accept Medicare or Medicaid reimbursement must be in compliance with the CMS Conditions of Participation (CoPs). This program will cover in detail the CMS requirements for hospitals to help prevent the hospital from being found out of compliance with the grievance regulations.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/2016-NEW-CMS-COP-REGULATIONS-GRIEVANCES-COMPLAINTS-501592/AUGUST-2016-ES-TRAININGREGISTRY
  • 97 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
  • 98 Request Info

    Webinar On Considerations for a Successful Biosimilars Program

    By 2020, the global biosimilars market is expected to surpass $6 Billion. From 2015 through 2020, 39 biologic drugs with combined U.S. sales of $41 B, roughly 30% of the market, will lose their marketing exclusivity. The result is increased interest in the biotech industry to gain entry into this potentially lucrative market. However, the combination of rigorous regulatory requirements, the potential for high manufacturing complexities, and innovative strategies by drug manufacturers to restrict entry of new players is restraining growth in this market.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/SUCCESSFUL-BIOSIMILARS-PROGRAM-501570/JULY-2016-ES-TRAININGREGISTRY
  • 99 Request Info

    Webinar On OCR Launches Phase 2 HIPAA Audits for Covered Entities and Business Associates: Are You Ready?

    Every Covered Entity and Business Associate is liable to be audited for HIPAA Compliance by U. S. Department of Health and Human Services (HHS). HIPAA Compliance Audits are now underway. HHS finalized HIPAA Compliance Audit procedures and is screening Covered Entities picked randomly from the National Provider Identifier (NPI) database to identify the first group of Covered Entities to be audited. The first group of Business Associates audited for HIPAA Compliance will be selected from Business Associates of the first group of Covered Entities. This is an enforcement audit.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/OCR-LAUNCHES-PHASES-2-HIPAA-AUDITS-BUSINESS-501578/JULY-2016-ES-TRAININGREGISTRY
  • 100 Request Info

    Webinar On Medicare Overpayments: Now what? What do you do and when do you do it?

    The course will cover all aspects of overpayment, identification of overpayment on the organizations part, overpayment and demand bills from Medicare. What to do if you believe the over payment demand is in error.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-OVERPAYMENTS-WHAT-DO-YOU-WHEN-DO-YOU-501449/JUNE-2016-ES-TRAININGREGISTRY