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Courses

  • 161 Request Info

    HIPAA Training for the IT Manager

    Overview: This webinar will be addressing how IT managers (and HIPAA Security Offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2019. Areas also covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information regarding the do's and don'ts with HIPAA - I want to add clarity for compliance officers and what you guys need to do and how to best implement your HIPAA program based on over 18 years of personal experience working with Federal auditors, state auditors, and corporate auditors.
  • 162 Request Info

    HIPAA Training for the Practice Manager

    Overview: This webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2019. Areas also covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information regarding the do’s and don’ts with HIPAA - I want to add clarity for compliance officers and what you guys need to do and how to best implement your HIPAA program based on over 18 years of personal experience working with Federal auditors, state auditors, and corporate auditors. We will go through multiple scenarios that are commonly faced by compliance officers and how to manage these situations
  • 163 Request Info

    HIPAA, 42 CFR Part 2, and FERPA - Rules for Managing Student Health Information

    This session will explore the complications and requirements of each of the rules controlling student health information, HIPAA, FERPA, and 42 CFR Part 2, and provide insights into how to apply the rules in an education setting.
  • 164 Request Info

    HIPAA, Consents, and 42 CFR Part 2 - Tracking the Release of Information Under Conflicting Rules

    Overview: For much of healthcare, HIPAA sets the standards for how to manage uses and disclosures of patient information, known as Protected Health Information (PHI). But when it comes to information related to the treatment of substance use disorders, regulations of the Substance Abuse and Mental Health Services Administration (SAMHSA) under 42 CFR Part 2 prevail, including rigorous controls on the release and re-release of patient information.
  • 165 Request Info

    Hosting FDA Regulatory Inspections 2018

    The course will go through what typically goes on during an FDA inspection and will then cover how to prepare for, host and follow up to a regulatory inspection. It will focus the things that you should do or not do during the inspection. Typically FDA inspections can be highly structured and there are usually procedures that are to be followed. It is important for anyone who might be involved in the inspection to be aware of these procedures.
  • 166 Request Info

    How the New Rules for the Sanitary Transportation

    Overview: This webinar is designed to help you understand how the new rules for the sanitary transportation of human and animal foods will impact your logistics operations and to provide you with some of the tools needed to meet new regulations and customer demands.
  • 167 Request Info

    How to Analyze Financial Statements 2019

    Overview: Grab a cup of coffee and join us to learn how to analyze the numbers, and use this intel to juice up virtually every facet of your organization's operations from marketing, to finance, to HR, to customer service and sales. Use our proven model to quickly assess the financial condition and results of operations of any business using trend and ratio analysis. Join C-suites and business analysts from around the country and empower your team to maximize the benefit from your crystal clear understanding of the numbers.
  • 168 Request Info

    How to be efficient and compliant with 21 CFR Part 11, data integrity, SaaS/Cloud, and EU GDPR

    This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.
  • 169 Request Info

    How to Compliance with SaaS/Cloud Software Applications

    Overview: It gets you on the right track for using electronic records and signatures to greatly increase productivity and ensure compliance. Areas Covered in the Session: Which data and systems are subject to Part 11 and Annex 11 What the regulations mean, not just what they say Avoid 483 and Warning Letters Requirements for local, SaaS, and cloud hosting SOPs required for the IT infrastructure
  • 170 Request Info

    How to Comply with New HIPAA Email and Text Message Rules and Avoid Danger

    Overview: Regular (unencrypted) Email and Text Messaging are effective engagement and communication tools that most patients prefer and have the right to use. HIPAA allows Providers and Business Associates on behalf of Providers to communicate with patients by unencrypted email and text message - but only when a simple 3 Step Safeguard is in place and documented.
  • 171 Request Info

    How to Conduct Effective Close out Meetings

    Overview: This webinar is designed to provide the participants a working knowledge of supplier audits. The why, when, who, how, and what of conducting a supplier audit will be reviewed to ensure that your supplier is capable of meeting all of your expectations. Why should you Attend: A good supplier audit program should allow an organization to assess and periodically re-affirm the ability of key suppliers to provide conforming product consistently, reliably and on-time. It should be one of the most important initiatives toward fulfilling the goal of having a sustainable supply chain.
  • 172 Request Info

    How to Conduct Medical Device Risk Analysis Effectively

    Why companies are prone to having past problems in new devices? One of the main reasons seems to be the ?weak cognition.? It is usually the result of short term memory, inattention to details, insufficient vigilance, or multitasking. This unsafe work propagates unknowingly because of not engaged or disengaged employees, insufficient understanding of customer needs, splitting design among several designers, and ineffective risk analysis. Another big reason is that ineffective device management procedures often touted as 'best practices', are like a bad virus with long incubation period and no early warning, resulting into sudden catastrophic malfunction of the device. Most companies still hold individuals responsible for mistakes instead of fixing the management process. Marketing has the advantage of helping prevent past mistakes and improve efficiency of the device design. They have records of customer complaints for years.
  • 173 Request Info

    How to Create a Medical Software Development File - ISO 62304

    Overview: This course will give an introduction how to develop medical software under the requirements of the ISO 62304 and how to apply these in a medical software development project and how a smart application during the medical software development and in the post market process is possible. Further the risk management of medical software development. In the European Union is the application of the ISO 62304 for medical software mandatory and part of the essential requirements of the medical device regulation. In the technical documentation is required to approve the development process and the life cycle of medical software according ISO 62304.
  • 174 Request Info

    How to Deal With the Disruptive Practitioner

    Disruptive activity by practitioners in the hospital takes many forms. When it happens, it is important that the hospital and/or the medical staff take appropriate steps to see that it does not affect patient care or disrupt operations. Hospital executives, medical staff officers, and peer review committee members and support staff should attend to learn how to deal effectively with the disruptive practitioner. You will also learn how to prepare for the day when it becomes necessary to terminate such a practitioner’s privileges and medical staff membership. You will also gain an understanding of how to develop provisions in the medical staff bylaws to deal with the disruptive practitioner and how to develop a clear and concise policy regarding disruptive behavior. We will discuss the elements of an effective policy and the actions that should be taken to develop progressive discipline and/or sanctions that should be taken before taking action under the corrective action procedures.
  • 175 Request Info

    How to Develop Predictive Warranty Using Paynter Charts

    Overview: Attendees will see how to actively utilize representative return data, observe the construction of a sample Paynter and then observe the results of the predictive analysis. Why should you Attend: Quality practitioners must understand how their VOC field return information can be leveraged to aid them in proactively mitigating risk and working across the supply chain when something goes wrong.
  • 176 Request Info

    How to Go Global: 5 Proven Foreign Market Entry Techniques

    Overview Due to cost advantages from producing overseas, revenue opportunities from foreign sales and the potential to exploit new technology, tapping international markets holds the greatest potential for growth.
  • 177 Request Info

    How to Maximize this Connection to Improve the Quality

    The objective of training is to transmit knowledge in such a way that learners are more inclined to remember it and use it effectively on the job. Often, when training is created based on an SOP, its content does not differ markedly from the SOP and tends to be dull. Therefore, when training is created based on the SOP, adult learning objectives are still important.
  • 178 Request Info

    How to Meet FDA QSR and ISO 13485 Requirements - 2017

    Overview: A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA does not directly regulate component suppliers, it is imperative that your company's purchasing and supplier control requirements provide the assurance that only acceptable components are used to manufacture finished devices.
  • 179 Request Info

    How to properly investigate OOS/OOT Results

    Overview The speaker will provide sound training on how to recognize and investigate atypical or out of specification results, using approaches which have been recommended by regulatory authorities, performing appropriate investigations. This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they are to be performed. The structure of an Investigation report which properly documents the investigation will be discussed. For more detail please click on this below link: http://bit.ly/2ru2Sae Email: referrals@complianceglobal.us Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510
  • 180 Request Info

    How to Register and Maintain Various Types of Combination Products | Seminar 2018

    A thorough understanding of the complexities involved Covers all the relevant regulations and guidelines Gives real life examples of how to register and maintain various types of combination products Interfaces: Change Management and LCM