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  • 41 Request Info

    Webinar On Steps to HIPAA Compliance and Ransomware Prevention

    This webinar will explain what the highest risk factors for being sued for wrongful disclosures of PHI are, and the manner in which patients are now using state laws to sue for wrongful disclosures. He will also delve into specific information about multiple incidents, which will help practices and businesses understand what they did wrong that led to a HIPAA risk of ransomware.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-RANSOMWARE-502761/APRIL-2017-ES-TRAININGREGISTRY
  • 42 Request Info

    Webinar On Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device

    This webinar ensures your company gets a broader perspective of how and what to do to get a quick and non-debatable or questionable approval for your 510K product. All are different so this presentation will not just be specific for a specified Medical Device that is currently being marketed and your company wants the same opportunity to produce and sell that product.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/US-FDA-MEDICAL-DEVICE-510k-508586/APRIL-2017-ES-TRAININGREGISTRY
  • 43 Request Info

    Webinar On OSHA Updates Guidance on Preventing Workplace Violence in Health Care, Social Services

    Does your healthcare facility know the full extent of the number of workplace violence episodes, or like most is the number vastly underreported? Do you know the costs of workplace violence and would like to reduce your costs exposure risk of lawsuits, reputation or OSHA audit? Are you in California and compliant with the new Cal-OSHA rules? 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/UPDATE-OSHA-GUIDANCE-503006/APRIL-2017-ES-TRAININGREGISTRY
  • 44 Request Info

    Webinar On Falsifying Data in Clinical Trials: What to Report?

    Falsifying data in clinical trials is also considered data fraud. When data fraud occurs there are most likely other unreported or undetected misconduct that occurred within a clinical trial. This leads to poor, unreplicable results. When results cannot be replicated, questions arise about why a trial was conducted and what types of risks or harms were the participants exposed to.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/FALSIFYING-DATA-CLINICAL-TRIALS-502132/MARCH-2017-ES-TRAININGREGISTRY
  • 45 Request Info

    Webinar On The Do's & Don'ts of Medical Record's Retention and Destruction

    Protect your organization from legal hardships concerning patient medical record privacy, security and management requirements. This topic is intended to be an overview of the general legal concepts applicable to medical records and destruction.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/DOs-DONTs-MEDICAL-RECORDs-506676/MARCH-2017-ES-TRAININGREGISTRY
  • 46 Request Info

    Webinar On How to Apply for a Breakthrough Therapy Designation and Win It

    This webinar, presented by a leading regulatory affairs expert with successful BTDs, discusses FDA expectations from BTD requests, the best practices to write a BTD request, and pros and cons of applying for a BTD. The session will highlight key regulatory requirements, dos and don'ts, common areas of concern, and trouble-shooting BTD requests using case studies and examples from the presenter's vast experience helping companies big and small in successfully applying for a BTD.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/BREAKTHROUGH-THERAPY-DESIGNATION-504525/MARCH-2017-ES-TRAININGREGISTRY
  • 47 Request Info

    Webinar On Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance

    This course provides a background to safety reporting. There is a refresher on the definitions and reporting requirements of AE, SAE, AR and SUSARs, within a clinical trial. We look at the sources of safety information and discuss the evidence that points to the causality of an event. The change in the regulatory environment is reviewed and the role of conditional approval and PASS and PAES studies is also 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/DRUG-SAFETY-PHARMACOVIGILANCE-504550/MARCH-2017-ES-TRAININGREGISTRY
  • 48 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
  • 49 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
  • 50 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
  • 51 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
  • 52 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
  • 53 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
  • 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 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
  • 56 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
  • 57 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
  • 58 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
  • 59 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
  • 60 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