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  • 21 Request Info

    Webinar On Medical Device Cleanliness: When and How to adjust LIMIT VALUES for Residual Analysis

    This webinar will provide valuable guidance to medical device manufacturers on how to establish and justify limit values for cleanliness. There are several techniques that may be used to set these limits, including comparison involving statistics and historical data. Justification techniques include biocompatibility and risk assessment. Regardless of what technique is used, regulatory agencies expect that limit values will be set for residual analysis.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/MEDICAL-DEVICE-CLEANLINESS-506851/AUGUST-2017-ES-TRAININGREGISTRY
  • 22 Request Info

    Webinar On Investigational Product Accountability Best Practices

    "An FDA inspector once said that any individual should be able to perform drug reconciliation at an investigative site within 20 minutes." (2002 Applied Clinical Trials). Conducting a clinical trial with a drug or device that is not FDA approved or that is being used in an investigational manner can be daunting. A site must know the federal regulations, and have accountability practices. All this can be very daunting.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/INVESTIGATIONAL-PRODUCT-ACCOUNTABILITY-503721/AUGUST-2017-ES-TRAININGREGISTRY
  • 23 Request Info

    Webinar On The DO's and DON'Ts of Social Media and HIPAA Compliance

    Hundreds of hospitals and other healthcare institutions across the nation are embracing social media. But how risky is this practice from a HIPAA and HITECH compliance stand point? Are you doing all you can/should to be compliant and manage/reduce the risk of a breach of PHI in your institution? By federal law PHI must be secured and its privacy insured. How do open very public forums like Facebook, Twitter and LinkedIn mesh with privacy and security?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/DOs-DONTs-SOCIAL-MEDIA-HIPAA-COMPLIANCE-504503/AUGUST-2017-ES-TRAININGREGISTRY
  • 24 Request Info

    Webinar On Protocol Deviations: Documenting, Managing and Reporting

    Deviations have often been misunderstood, misclassified and misreported. This webinar will help you to answer questions about deviations such as: What is a deviation? What’s the best way to manage deviations? Can they be avoided? What is their importance? Does deviations impact subject safety or data integrity? How can the research team anticipate, manage, and minimize the impact of protocol deviations?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/PROTOCOL-DEVIATIONS-502254/JULY-2017-ES-TRAININGREGISTRY
  • 25 Request Info

    Webinar On Techniques for Navigating Challenging Conversations at Work

    Difficult conversations between managers and employees are oftentimes dreaded. There are techniques that can be used to help in these challenging times. Knowing the right techniques can help you approach the conversation with confidence. Many people will avoid or put off a necessary conversation hoping that they will not have to ever have it, however, the issues will most likely not go away and they will have to be addressed at some point.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/NAVIGATING-CHALLENGING-CONVERSATIONS-WORK-508781/JULY-2017-ES-TRAININGREGISTRY
  • 26 Request Info

    Webinar On Nursing: CMS CoP Standards for Hospitals and Proposed Changes: 2017 Update

    This session by expert speaker Sue Dill Calloway, RN, MSN, JD, is a must attend for any clinical nurse or nurse leader or person interested in ensuring compliance with the CMS hospital conditions of participation in nursing. There has been an increase in surveillance and scrutiny in recent times to ensure that every hospital is in compliance with the hospital CoPs. Don't take chance and put your hospital's reimbursement at stake.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/2017-NURSING-CMS-CoP-HOSPITALS-508463/JUNE-2017-ES-TRAININGREGISTRY
  • 27 Request Info

    Webinar On OIG Work Plan 2017 - Hospital and Physician Audit Activities

    Every year the OIG updates what its focus is for the upcoming year. During this session we will look at the focus for OIG audits and oversight for 2017. These work plans often drive the audits that then occur within our work sites. They provided information that is beneficial for organizations in their striving to be compliant with new regulations.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/OIG-WORK-PLAN-2017-502738/JUNE-2017-ES-TRAININGREGISTRY
  • 28 Request Info

    Webinar On Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations

    Did you know that Electronic Health Record (EHR) can be used in prospective clinical investigations of human drugs, biologics, medical devices and combination products regulated by the US Food and Drug Administration (FDA)? This includes foreign studies used in support of an application for marketing approval of the medical product. This webinar will discuss FDA's current recommendations on using Electronic Health Records in prospective clinical investigations of human drugs, biologics, medical devices and combination products. A refresher on key requirements for Computer Systems used in Clinical Investigations is also included.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/EHR-FDA-CLINICAL-INVESTIGATIONS-505427/JUNE-2017-ES-TRAININGREGISTRY
  • 29 Request Info

    Webinar On CE Mark - Required to Sell Medical Devices in the EU

    This interactive webinar will address the circumstances that regulate medical device sales in the EU. Use of the CE Mark for medical devices is required for selling medical devices in the EU. The webinar will address the use of CE Marking and cover the process of marking which provides an indication of whether the product is in compliance with EU regulations to further allow product commercialization throughout the EU.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/CE-MARK-SELL-MEDICAL-DEVICES-EU-508084/JUNE-2017-ES-TRAININGREGISTRY
  • 30 Request Info

    Webinar On Compliance with ICH GCP R2 Addendum for Auditors

    This New ICH GCP E6 Revision 2 changes will cover those new requirements for running clinical trials, evaluate the changes and discuss how to implement these for sponsors, CROs and study sites. This session will enable you to meet the new international GCP standard to ensure the acceptance of clinical trial data by the regulatory authorities internationally including the European Union (EU), Japan, the United States, Canada and Switzerland.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/COMPLIANCE-ICH-GCP-R2-ADDENDUM-AUDITORS-505313/JUNE-2017-ES-TRAININGREGISTRY
  • 31 Request Info

    Webinar On Technical File Structure according to New EU Medical Device Regulation

    This course describes the structure and content of a technical file and its main attachments for the CE marking of a medical device.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/EU-MEDICAL-DEVICE-REGULATIOIN-504418/JUNE-2017-ES-TRAININGREGISTRY
  • 32 Request Info

    Webinar On The ABC's of Healthcare Reform: How to Be Successful Given the Changing Health Policy Landscape

    This webinar will provide an in-depth understanding of the future of healthcare reform and its implications. We will provide a comprehensive overview of payment and delivery system reform (key approaches to incentivize quality and value), and highlight the core drivers behind health reform, including healthcare consumerism, a focus on population health, stronger use of HIT data to drive improvements and better decision-making, and patient engagement.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/THE-ABC-HEALTHCARE-REFORM-502184/MAY-2017-ES-TRAININGREGISTRY
  • 33 Request Info

    Webinar On 2017 CMS Proposed Changes to the Discharge Planning Standards and the IMPACT Act

    CMS penalized 2,597 hospitals in FY2017 on account of unnecessary readmissions. This year the CMS under HRRP will withhold $528 million in payments in 2017, an all-time high and an increase of about $108 million from FY 2016. New evidence-based research is coming out every day on recommendations to help reduce unnecessary readmissions. But what can a hospital do to prevent unnecessary readmissions?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/2017-CMS-PROPOSED-CHANGES-IMPACT-ACT-503749/MAY-2017-ES-TRAININGREGISTRY
  • 34 Request Info

    Webinar On Benefit and Risk Factors to be considered for managing the FDA IDE (Investigational Device Exemption) Submission for Medical Devices

    Key benefit and risk factors to be considered while submitting an investigational device exemption (IDE) to FDA will be discussed in this webinar. IDE submission allows the investigational device to be used in a clinical study in order to collect safety and effectiveness data required to support a Premarket Approval (PMA) application or a Premarket Notification [510(k)] submission to FDA.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link
  • 35 Request Info

    Webinar On Medical Device Reporting Requirements for Manufacturers Final Guidance

    This webinar explains the MDR regulation considering the new information contained in the Guidance and describes a compliant MDR procedure. Areas covered will include death, injury and mal-function reporting requirements, record keeping requirements, report timing, clarification of the term ‘becoming aware’ and clarification of reporting using electronic form 3500A.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/FDA-MDR-REGULATION-506828/MAY-2017-ES-TRAININGREGISTRY
  • 36 Request Info

    Webinar On Changes to the Common Rule (45 CFR 46): What this Means for You

    45 CFR 46 is called the Common Rule because a number of different federal agencies agreed to abide by this rule when conducting human subjects' research. This regulation came out of a national commission charged with reviewing instances of research involving humans where the research participants were not treated appropriately as per the existing ethical codes of the time: The Nuremberg Code and the Declaration of Helsinki.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/COMMON-RULE-45-CFR-46-504172/MAY-2017-ES-TRAININGREGISTRY
  • 37 Request Info

    Webinar On What Physicians Need to Know about MACRA - But Were Afraid To Ask!

    In this session, our expert speaker Mr. Wolfe will provide an overview of the Quality Payment Program, including its MIPS and Advanced APM pathways. Mr. Wolfe will provide a straight-forward, practical explanation of key provisions and options for clinicians and health care leaders as they navigate the 2017 transition year and beyond.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/MACRA-CMS-QUALITY-PAYMENT-PROGRAM-503864/APRIL-2017-ES-TRAININGREGISTRY
  • 38 Request Info

    Webinar On Regulatory Challenges Facing In-Vitro Diagnostic in U.S.

    In-vitro diagnostic (IVD) products drive a significant portion of clinical decision making today. IVDs assist in the identification, diagnosis and monitoring of disease. They play an ever-expanding role in the selection of appropriate therapeutic interventions in healthcare delivery with the advent of personalized medicine. These key products are a distinct class of medical devices regulated in the US by the Food and Drug Administration (FDA).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/REGULATORY-CHALLENGES-VITRO-DIAGNOSTIC-US-508213/APRIL-2017-ES-TRAININGREGISTRY
  • 39 Request Info

    Webinar On Compliance with EU Regulation for Clinical Trials

    This webinar will help ensure attendees are familiar with new regulations for running clinical trials in Europe. It will help them prepare to implement the new requirements efficiently while elaborating how clinical trials will be authorized in the future. The instructor will also detail the authority proffered to EU regulators to perform inspections of all clinical trials registered in the EU, whether they are conducted within the EU or internationally in other emerging markets.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-EU-REGULATION-CLINICAL-TRIALS-506624/APRIL-2017-ES-TRAININGREGISTRY
  • 40 Request Info

    Webinar On Medical Device Recalls: a Preventive Strategy

    The secret to preventing medical device recalls is to implement and follow basic practices for specifications and design control, design for process reliability, production validation and design validation using accelerated life tests. This webinar is about controlling safety risk from specification writing to device retirement - control throughout the product's life cycle.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/MEDICAL-DEVICE-RECALLS-509325/APRIL-2017-ES-TRAININGREGISTRY