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  • 41 Request Info

    Webinar On OASIS C-2: Are you Prepared for the upcoming Changes Effective 1st January 2017?

    This session by expert speaker Sharon Litwin, RN, BS, MHA, will ensure that you are aware of new changes in OASIS C2. Sharon will also address some important home health topics such as Star ratings, value based purchasing, reimbursement and outcomes in this presentation. Additionally, you will also receive OASIS C2 data set along with the presentation.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/OASIS-C-2-501927/DECEMBER-2016-ES-TRAININGREGISTRY
  • 42 Request Info

    Webinar On Lean Healthcare Facility Design

    Everyone knows we must focus on safety in healthcare delivery. Attending this session will help you better understand how the built environment impacts safety and is integrated with operational efficiencies.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/LEAN-HEALTHCARE-FACILITY-DESIGN-501911/DECEMBER-2016-ES-TRAININGREGISTRY
  • 43 Request Info

    Webinar On CMC Considerations for Successful Regulatory Submission

    This webinar is intended to provide advice on the level of detail required for regulatory submissions at different program phases. Regulatory strategy across the development program will also be discussed.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/CMC-REGULATORY-SUBMISSION-501931/DECEMBER-2016-ES-TRAININGREGISTRY
  • 44 Request Info

    Webinar On Chronic Care Management: Boosting Revenue of your Practice and Improving Patient Care

    This course will explain in detail the Medicare Chronic Care Management initiative. Medicare estimates that approximately two thirds of all Medicare patients are eligible for this program. Medicare will pay clinicians an average of approximately $43 a month for providing 20 minutes or more of non-face-to-face management services for patients with two or more chronic medical conditions.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/CHRONIC-CARE-MANAGEMENT-501936/DECEMBER-2016-ES-TRAININGREGISTRY
  • 45 Request Info

    Webinar On Inclusion of LGBT Employees in Healthcare: Navigating Policies, Procedures, and Practices

    How does your business go about recruiting to the LGBT community? Do any of your advertising and marketing practices target LGBT consumers? Do you know how to assist a transgendered employee in their gender transition process at work? And what about those bathrooms—how are you addressing this issue? Workplaces have made progress towards LGBT equality yet LGBT workers still go to work every day with fear that they might lose their jobs because of whom they love and who they are.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/LGBT-EMPLOYEES-HEALTHCARE-501959/DECEMBER-2016-ES-TRAININGREGISTRY
  • 46 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
  • 47 Request Info

    Webinar On Importance of Usability in Medical Device Procurement

    The FDA has progressively increased requirements for human factors and usability testing before new medical devices can be approved for market release. However, successful market release does not ensure a device is easy to use or that all potential for safety-critical errors has been mitigated. Medical device purchasers must consider incorporating human factors as a standard part of the procurement process to ensure that they are choosing the safest, most usable devices for purchase.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-DEVICE-PROCUREMENT-501983/DECEMBER-2016-ES-TRAININGREGISTRY
  • 48 Request Info

    Webinar On Ensuring Compliance with ICH GCP E6 (R2) Requirements: Meeting the challenges of RBM

    This training will look at the principles of risk management and how they apply in RBM. We will look at the changing regulatory environment with a focus on the changes outlined in ICH GCP E6 (R2) and how these changes may impact your clinical trials.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-ICH-GCP-E6-R2-501987/DECEMBER-2016-ES-TRAININGREGISTRY
  • 49 Request Info

    Webinar On Good Post-Market Surveillance

    Post-Marketing Surveillance (PMS) is the practice of monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and is an important part of the science of pharmacovigilance. The purpose of post-market surveillance is to protect individual health and public health through continued surveillance of products once they are placed on the market by reducing any risks.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/GOOD-POST-MARKET-SURVEILLANCE-501998/JANUARY-2017-ES-TRAININGREGISTRY
  • 50 Request Info

    Webinar On The Sunshine Act: Reporting for Clinical Trials

    The Sunshine Act exposes the physicians and sponsors to new reporting requirements which are unprecedented in their scope and detail noncompliance to which would lead to hefty fines. This webinar will summarize the new requirements and provide practical solutions to most common situations that are prevalent and necessary between sponsors and investigators.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/SUNSHINE-ACT-CLINICAL-TRIALS-502017/JANUARY-2017-ES-TRAININGREGISTRY
  • 51 Request Info

    Webinar On Requirements for Registration of Medical Device Products in China

    China's medical device market is rapidly growing these years, China offers numerous opportunities for foreign healthcare related companies but understanding the practicalities of accessing the market is not simple. Attend this training, if you are a manufacturer or distributor involved in exporting medical devices or IVDs to China, this webinar will provide you with necessary briefing on CFDA registration of medical devices.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-PRODUCTS-CHINA-502010/JANUARY-2017-ES-TRAININGREGISTRY
  • 52 Request Info

    Webinar On Best Practices for Effective Pharma Technology Transfer: From R&D to Clinical to Commercial

    This webinar discusses effective Pharmaceutical Technology Transfer procedures as they are currently practices by successful pharmaceutical and biopharmaceutical firms. It introduces compliant modular approach to technology transfer projects that covers multiple disciplines including Project Management, Analytical and Microbial Quality Control, Operations, Quality Assurance Safety, Engineering, Regulatory Affairs and other relevant areas.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/PHARMA-TECHNOLOGY-TRANSFER-502023/JANUARY-2017-ES-TRAININGREGISTRY
  • 53 Request Info

    Webinar On Challenges with the NOTICE Act and the MOON Form: Is your Hospital/CAH Facility Ready for the Upcoming March 8 Implementation

    CMS has recently posted its updated version of the Medicare Outpatient Observation Notice (MOON), a standard notice that all hospitals and critical access hospitals must provide to Medicare beneficiaries who receive outpatient observation services for more than 24 hours. All hospitals and critical access hospitals (CAHs) are required to provide the MOON beginning no later than March 8, 2017.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/CHALLENGES-NOTICE-ACT-MOON-FORM-502058/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 54 Request Info

    Webinar On HIPAA Compliance in 2017: Changes under Omnibus Rule and Best Practices

    This training will address 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 2017 and beyond. There are an enormous amount of issues and risks for covered entities and business associates these days.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-COMPLIANCE-2017-502062/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 55 Request Info

    Webinar On Strategies to increase your MIPS Performance Score and How to Achieve "Bonuses" for Exceptional Performance

    If you are looking for a help with understanding how the MIPS score is determined and how your practice can achieve "bonuses" in the form of exceptional positive payment adjustments, this course is for you. We will explore how the score is generated from each MIPS performance category and how to overcome performance barriers.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/MIPS-PERFORMANCE-SCORE-503771/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 56 Request Info

    Webinar On Clinical Trial Best Practices: Avoid unnecessary filings of Notes to File (NTF) in your TMF

    Notes to File (NTF), also known as Memo to File, are commonly used as essential documentation in sponsor and site files. Many times the content of the NTF does not serve the purpose for use or serves no purpose at all. This webinar will discuss the appropriate and inappropriate uses of NTF, the questions to ask to determine if NTF would be beneficial, and the components of a quality NTF, if being used.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-BEST-PRACTICES-506962/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 57 Request Info

    Webinar On CMS Hospital Improvement Act Proposed Changes: Nursing, Medical Records, Infection Control, Antibiotic Stewardship Program, Restraints, QAP

    CMS has proposed some significant changes to the hospital conditions of participation (CoPs) that every hospital should know including critical access hospitals. This includes changes to nursing, medical records, infection control, QAPI, patient rights and restraint and seclusion. It will also require all hospitals to have an antibiotic stewardship program and what the program should includePrice:$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/CMS-HOSPITAL-ACT-PROPOSED-CHANGES-508562/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 58 Request Info

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

    The recommended and required contents of the trial master file (TMF) continue to be a concern for clinical trial professionals. All companies and investigators conducting clinical trials in the pharmaceutical/biotech industry maintain documentation for each clinical trial. Each company has their own unique TMF structure as defined by their SOPs however many are not clear on the regulatory expectations.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-TMF-505044/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 59 Request Info

    Webinar On Powers of Attorney: Medical Records Release Concerns

    This live webinar will educate you on how to identify a valid power of attorney to determine whether information should be disclosed. Additional discussions will be held on other issues surrounding access to patient health information such as health care proxies and subpoenas. You need to understand the nuances of patient information requests and the authority you can rely on when turning over patient health information.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/POWER-ATTORNEY-MEDICAL-RECORDS-507407/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 60 Request Info

    Webinar On Final Rule Home Health Conditions of Participation (HHCoPs): Impact and Implications for Home Health Agencies

    In this training, Speaker Sharon Litwin will discuss her analysis of the Home Health Conditions of Participation Final Rule and their potential impact and implications for home health agencies. 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/FINAL-RULE-HHCoPs-507148/FEBRUARY-2017-ES-TRAININGREGISTRY